CA1175811A - Diazonium sulfonates and uses thereof - Google Patents

Abstract

ABSTRACT OF THE DISCLOSURE

Provided are novel light-sensitive diazonium compounds known as diazonium trifluoromethane sulfo-nates, which have the structural formula:

wherein

Description

lO75~1 DIAZONIUM SULFONATES AND USES THEREOF

BACKGROtJND OF THE INVENTION
. _ Field of the Invention:
This invention relates to novel light-sensitive diazonium compounds, their preparation anduses thereof. More particularly, the present invention pertains to diazonium trifluoromethane sulfonates and formulations comprising same employable in diazotype materials. In another aspect of the present invention, said diazonium trifluoromethane sulfonates are useful as latent polymerization initiators for the photopoly-merization of a polymeriæable system.

Description of the Prior Art:
Diazotype photoreproduction is, of course, a standard in the graphic arts. The touchstone of diazography processes is the light-sensitivity of aromatic diazo salts and the fact that such salts undergo two different types of reactions: [11 replace-ment or decomposition, in which nitrogen is lost or evolves as nitrogen gas and some other atom or group attaches to the benzene ring in its stead; and [21 "coupling", wherein the nitrogen of the diazo ~unction is retained and the salts react wlth cer~ain couplable color-forming components, i.e., a "coupler" or "azo-coupling component", to effect Eormation of an azo dyespecies.
In positive-working diazo processes, a light-sensitive diazo-salt composition, which sensitizing formulation generally comprises a diazo compound, a coupling component or color former, and an acidic '' ~.

1 1~58~1 coupling inhibitor, is applied to a carrier or base, which may be paper or a transparent film such as cellu-lose acetate or a plastic coated base support, to form a positive-working material. The posi~ive-working material is imaged by first exposing it through a master transparency or original. The light in the exposure step must supply sufficient energy to destroy the diazo compound in the areas corresponding to the clear background of the original.
The photochemical sensitivity of compounds typically employed in diazotype photographic repro-duction materials resides in the near-ultraviolet region of the spectrum, and is centered about 400nm (nano~eters), one nm being equal to a millimicron or 10-9 meter; thus, medium-pressure, metal halide mercury lamps are generally used in performing this step. As a result, that part of the diazo coating which is unpro-tected from the ultraviolet radiation by the ;mage of the original becomes a colorless substance, incapable of coupling with the "coupling" component, which is generally an aromatic amine, phenol, or aliphatic com-pound containing active methylene groups, to form colored oxyazo or aminoazo compounds known as azo dyes. The unaffected diazo compound which remains in those areas where the light has not struck, hawever, is able to form an azo dye by reaction with the coupling component when the medium is made alkaline to neutralize the acidic inhibitor. Thus, wherever there was an opaque line on the original, a dye-line appears on the copy. Positive-working, diazotype photore-production material is generally made alkaline, or pH
adjusted, either by impregnating the material with ammonia vapors or passing it through an alkaline developing solution. See generally U.S. Patent Nos.
1,~44,469; 1,628,~79; 2,217,189; 2,286,701; 2,429,249 ~ 175~1 and 2/694~009; German Patentschriften Nos 5S,606:
111,416; 487,247 and 515,205; British Patent Specifica-tion Nos. 234,818; 281,604 and 521,492.
In sensitizing formulations! the diazos are usually in the form of stabilized compounds of acidic salts such as zinc chloride, cadmium chloride, stannic chloride, and tetrafluoroborate salts, as well as hexa-fluorophosphate salts. These salts are used to stabilize the diazo and also to enhance the keeping quality or shelf life of sensitized diazotype material.
It is also the general practice to provide some means of inhibiting print discoloration and image fading. To achieve this end, various additives are generally used in diazo formulations, such as thiourea, thiourea derivatives and other similarly~act}ng compounds.
Notwithstanding the use of various stabi lizers and additives in diazotype formulations, stability or shelf-life characteristics of diazotype materials have not been entirely satisfactory, particularly in diazotype materials sensitized with formulations employing diazos noted for their high coupling a~tivity and/or instability.
Moreoverr in formulating a sensitizing formulationl the greater the solubility of the diazos in the solvent system, the less solvent generally required to obtain the desired or predetermined amount of diazo in solution and the less likely problems with phenomena such as "blushing" are encountered. As well, the greater the solubility of the diazo, t.he higher the possible loading thereof in the solvent system, which, of course, provides for a denser image. Thus, the greater the solubility of a light-sensitive diazo compound, the greater the practical and economical convenience in using same.

The characteristic photodecomposition of certain aromatic diazo salts has also resulted in such salts being applicable in the role of a latent polymerization initiator for polymerizable systems such as those described in U.S. Patent Nos. 3,816,279;
3,816,280; 3,816,281; 3,817,845; 3,817,850; 3,835,003;
3,997,344; 4,~54,451; 4,054,452; 4,054,732; 4,056,3~3;
4,076,536; 4,080,274; and 4,091,194. Of course, diazonium salts which can be successfully employed in diazotype photoreproduction systems and, additionally, as latent polymerization initiators, possess increased commercial value due to their multiple important utilities.
Accordingly, a principal object of this in-vention is to provide novel salts of diazo compounds which can be employed to provide improved ligh~-sensitive diazo formulations.
Another object of this invention is to provide novel diazo salt compositions having improved stability, shelf-life and compatability with plastic materials which are used as supports in diazotype photoreproduction materials.
A further object is to provide a diazo salt employable in not only a positive-working diazography system, but also in a negative-working diazography system.
Still, a further object of this invention is to provide a novel diazonium compound of increased solubility in organic solvents.
Yet another object of the present invention is to provide a diazonium compound which is also a suitable latent polymerization initiator for the photo-polymerization of certain polymerizable systems.
Another important object of this invention is to provide an economical method of preparing a variety ~ 175~1 of diazo salt compoundsr and to make practical the commercial utilization of many diazosr which have here-tofore been considered uneconomical or difficult to manufacture.
Still another object of this invention is to provide improved diazotype photoreproduction materials and processes employing same.
Other objectsr features and advantages will become apparent to those skilled in the art upon a study of this disclosure and the appended claims.

SUMMARY OF THE INVENTION
:

The aforementioned objects of the present invention are realized by means of certain novel diazonium salts. Thus, in accordance with this invention, there are provided novel, light-sensitive diazo compounds, which compounds are diazonium trifluoromethane sulfonates, also referred to herein as diazonium triflates, i.e., the trifluoromethyl sulfonic acid salts of diazo compounds, and a method for preparing same.
In another embodiment of the invention there is provided diazography formulations comprising a diazonium triflate (a diazonium salt of trifluoromethyl sulfonic acid), a diazo coupling component, and an acidic coupling inhibitor, which diazography formu:La-tion is useful in providiny diazotype light~sensitive materials comprising a sheet material sensitized with said formulation.
Another embodiment of the invention pertains to a diazography composition comprising a novel diazonium triflate compound and an enolic, preferably phenolic, blocked-coupler or precursor of an azo coupling component adapted to be converted in the ~ 17581~

presence of an acid to an active azo coupling compo-nent~ which composition is applicable to diazotype material comprising a sheet material sensitized with said composition. Such diazotype material is u~eful in negative-working diazotype photoreproduction.
A further embodiment of the present invention includes the use of diazonium triflates as latent poly-merization ;nitiators in compositions comprising the t~iflate and cyclic ester, e.g., lactone; a monomeric or prepolymeric epoxide; a cyclic ether such as an oxetane; or mixtures thereof; for the subsequent polym-erization of said composition to higher molecular weights upon exposure to irradiation.

DETAILED DESCRIPTION OF THE PREFERRBD EMBODIMENTS

More particularly, the novel diazonium triflates of the present invention are the trifluoro-methyl sulfonic acid salts of a diazo compound, which can be represented by the following general formula:
o ~D~-N- ~ ~ -S-CF3 O
wherein ~ - N=N- is the cation of an organic diazonium compound~ i.e., the cation of any diazonium compound, and in particular, known diazonium compounds used in diazography formulations for diazotype photoreproduc-tion, e.g., such as those diazonium compounds disclosed in U.S. Patent Nos/ 2,661,291; 2,~94,010; 2,727,820;

2,8~1,065; 2,94~,~13; 3,082,200; 3,134,675; 3,164,~68;

3,203,803; 3,255,011; 3,386,828; 3,407,066; and 3,816,280. Accordingly, ~ can be any unsubstituted or substitu~ed mono or polycyclic aryl or heterocyclic aromatic, hut is preferably selected from the group consisting of unsubstituted or substituted phenyl, .

.

1 ~75~

naphthyl, anthryl, phenanthryl and azaheterocyclic aromatic moieties. Exemplary substitutents thereof are those selected from the group consisting of, for example, an alkyl, alkylamino, dialkylamino, arylamino, aralkylamino, phenoxy, phenyl, phenyl thio ether, morpholino, piperidino, pyrrolidino, hexamethylene-imino, halide, alkoxy, cycloalkyl and piperaæino radical. The type, position and number of substituents are without restriction, except of course, for generally applicable chemical principles. Most likely, same will be determined or chvsen in accordance with the ultimate utility of the diazonium triflate. Para-substituted compounds, in general, have been found to be most useful and applicable to diazography utili--ties. Further, the preferred alkyl and alkoxygroupings are lower alkyl and alkoxy having from 1 to about 8 carbons; the preferred aryl groupings are of 5 to about 10 carbons; and, the preferred cycloalkyl groupings are of 3 to about 8 carbons. Illustrative of an azaheterocyclic aromatic moiety is a pyridy1 radical, e.g., an aminopyridine derivative.
; The diazonium triflates are prepared as the reaction product of trifluoromethyl sulfonic acid, or a salt thereof, and a diazonium compound.
The trifluoromethyl sulfonic acid, or salt thereof, used to prepare the diazo salt of the present invention may be in the form of the acid or any of its salts, and is most preferably in a form which is more soluble in the reaction medium than the diazo trifluoromethane sulfonate (diazo triflate) being prepared. The trifluoromethyl sulfonic acid reactant can be represented by MOS02CF3, wherein ~ represents hydrogen, metallic or other cation, as for example, K, Na or ammonium salts.

~ ~7S8~

The diazonium compounds which may be used in accordance with the pre~ent invention to react with the triflate can be represented by the general formula:
~ -N=NX, wherein ~ N=N- is the same as before and X
represent~ an anion capable of producing a stable ; diazonium compound. Basically, any diazonium compound, and in particular, known diazonium compounds used in diazography formulations for diazotype photore-production, can be employed, e.g., such as those diazonium compounds disclosed in the aforelisted U.S.
Patents. Exemplary diazonium compounds include those formed from the following lists of exemplary cations -N = ~ and anions ( ~ , which lists are not meant to be limitative.

CATIONS:
(1) p-chlorobenzenediazonium;
(2) 2,4-dichloroben2enediazonium;
(3) 2,5-dichlorobenzenediazonium;

(4) 2,4,6-trichlorobenzenediazonium;

(5) p-methoxybenzenediazonium;

(6) o-methoxybenzenediazonium;

(7) 2-chloro-4-(dimethylamino)-5-methoxybenzenediazonium;

(8) 4-chloro-2,5-dimethoxybenzenediazonium;
~9) 2,4',5,-triethoxy-4-biphenyldiazonium ~2,S-diethoxy-4-(p-ethoxyphenyl)benzenediazOniUml;
(10) 2,5-dimethoxy-4'-methyl-4-biphenyldiazonium [2,5-dimethoxy-4-(p-tolyl)benzenediazOniUml;
(11) 2,5-diethoxy-4 (phenylthio)benzenediazonium;
(12) 2,5-diethoxy-4-(p-~olylthio)benzenediazonium;
(13) p-morpholinobenzenediazonium (14) 2,5 dichloro-4-morpholinobenzenediazonium;
(15) 2,5-dimethoxy-4-morpholinobenzenediazonium (16) 4-(dimethylamino)naphthalenediazonium;

~17~
_9_ (17) 4-N,N-dimethylaminobenzenediazonium;
(18) 4-N,N diethylaminobenzenediazonium;
(19) 4-N-ethyl~-N-hydroxyethylaminobenzenediazonium;
(20) 4-N-methyl-N-hydroxyethylaminobenzenediaæonium;
(21) 4 N-ethylaminobenzenediazonium;
(22) 4-N,N-diethylamino-2-methylbenzenediazonium;
(23) 4-N-ethyl-N-benæylaminobenzenediazonium;
(24) 4-N,N-diethylamino-3-chlorobenzenediazonium;
(25) 4-N-morpholino-2,5-diethoxybenzenediazonium;
(26) 4-tP-tolylthio)-2,5-diethoxybenzenediazonium;
(~7) 4-(p-chlorophenoxy)-2~5-diethoxybenzenediazonium;
: (28~ 4-(p-ethoxyphenyl~-2,5-diethoxybenzenediazonium, (29) 4-N,N-bis( ~-hydroxyethyl)aminobenzenediazonium;
(30) 4-N-pyrrolidino-3-methylbenzenediazoniu~;
(31) 4-N(2,6-dimethylmorpholino)benzenediazonium;
(32) 4-N-piperidinobenæenediazonium;
(33) 4-M-pyrrolidinobenzenediazonium;
(34) 4-N-hexamethyleneiminobenzenediazonium;
(35) 4-N-piperazinobenzenediazonium;
(36) 4-N-(N'-methylpiperazino)benzenediazonium;
(37) 4-N-{N-(3-azabicyclo[3.2.2]nonane)}benzene-diazonium;
(38) 4-N-~NL~-hydrox~ethyl)piperazino]benzene-diazonium;
(39) 4-N~(N'-acetylpiperazino)benzenediazonium;
(40) 4-N-morpholino-2,5-diisopropoxybenzenediazonium;
(41) 4-N-azacycloheptane-2,5-diethoxybenzenediazonium;
(42) 6-dimethylamino-3-pyridinediaæonium;
(43) 6-diethylamino-3-pyridinediagonium;
(44) 6-methylamino-3-pyridinediazonium;
(45) 6-ethylamino-3-pyridinediazonium;
~46) 6-morpholino-3-pyridinediazonium (47) 6-piperazino-3-pyridinediazonium;
(48) S-benzylamino-3-pyridinediazonium;
(49) 6-p-toluidino-3-pyridinediazonium;

1 175~ll (50) 6-(p-dimethylaminoanilino) 3-pyridinediazonium;
(51) N,N'-(4,4'-biphenylene)bis(6-amino-3-pyridinediazonium);
(52) 6-anilino 3-pyridinediazonium;
(53) 6-(2-pyridylamino)-3-pyridinediazonium (54) 6,6'-(p,p'-methylenedianilino)bis(3-pyridinediazonium);
(55) N-methyl-6-anilino-3-pyridinedlazonium;
(56) 6-dimethylamino-5-methyl-3-pyridinediazonium;
(57) 2-dimethylamino-3-pyridinediazonium;
(58) 4-N,N-diethylamino-2-ethoxybenzenediazonium;
(59) 4-N ethylamino-2-methylbenzenediazonium;
(60) 4-N,N-bishydroxyethylbenzenediazonium;
(61~ 4-N-oxazolidinobenzenediazonium;
(62) 4-N-methyloxaæolidinobenzenediazonium;
(63) 4-N-(tetrahydro 1,3-oxaæino)benæenediazonium;
(64) p-ethoxybenzenediazonium;
(653 3-chloro-4,6-dimethoxybenzenediazonium;
(66) p-acetamidobenzenediazonium;
(67~ 4-bromo-2r5-diethoxybenzenediazonium;
(68) 4-N-benzylamino-2-methoxy-5-methylbenzenediazonium;
(69) 4-N-benzoylamino-2-methoxy-S-methylbenzenediazonium (70) 4-N-phenylthioacetylamino-2,5-diethoxybenzene-diazonium;
: ~71) 4'-acetylamino-2,5-diethoxy-4-biphenyldiazonium;
(72) 4-N-piperidino-5-methoxy-2-(p-tolylthio)benzene-diazonium;
(73) 4-~p-~olylthio)-5-methoxy-2-piperidinobenzenedia-zonium;
(74) 4-N-morpholino-5-mekhoxy-2-(p-tolylthio)benzenediazonium;
(75) 4-N-piperidino-5-methoxy-2-piperidinobenzenediazonium;

.
.

~ ~ 75~

(76) 4-N-piperidino-5-butoxy-2 (p-tolylthio)benzenediazonium;
(77) 4-N-piperidino-5-methoxy-2-phenoxybenzenediazonium;
(78) o-nitrobenzenediazonium;
(79) p-nitrobenzenediazonium;
(80) 4-nitro-2-methylbenzenediazonium;
(81) 4-methyl-2~nitrobenzenediazonium;
(82) 2,4-dimethyl-6-nitrobenzenediazonium;
(83) 3-chloro-4-pyrrolidinobenzenediazonium.
(84) 4-morpholino-3-methoxybenzenediazonium;
(85) 4-N-benzoylpiperidino-2,5-diisopropoxybenzene-diazonium.

The preferred aromatic diazonium cations are those which, upon combination with the trifluoromethylsulfonate anion, ~ S02CF3, readily form a precipitate, i.e., a reaction product which is insoluble in the reaction medium, which is generally water. Examples of diazonium cations which do form largely water insoluble triflates are the 4~p-tolylthio)-2,5-diethoxybenzenediazonium: 4-N-morpholino-2,5-diisopropoxybenzenediazonium; and, 4-N-azacycloheptane-2,5 diethoxybenzenediazonium cations.
of course, the preference of any aromatic diazonium cation will ultimately depend upon the utility to which the diazonium triElate is destined. Indeed, if the diazonium triflate need exhibit some water solubility, then cations such as 4-N-ethyl-N-hydroxyethylaminobenzenediazonium and 4-N,N-diethylamino-2-methylbenzenediazonium would be more appropriate that the three aforenoted cations.
Among the specific cations listed above, those numbered (11), ~12), (15~, (24), ~25), ~30), ~34), ~40), ~74), ~77), ~84) and ~85) are presently preferred.

~ ~75~11 Anions:
(1) tetrafluoroborate,BF4 (2) hexafluorophosphate,PF6~
(3) hexafluoroarsenate(V),AsF6 (4) hexafluroantimonate(V),SbF~~ ;
(5) pentachlorobismuthate(III),BiC15 2 (6) trichlorostannite,SnC13~
t7) trichlorozincate~zn ; (8) chloride, Cl- ;
(g) sulfate, S04-2 (10) tetrachlorozincate/ ZnCl,~~2 (11) hexachlorostannate (IV),SnC16 2 (12) tetrachloroferrate (III), FeC14 (13) cadmium chloride, CaC14 2 (14) bisulfate, HSO~ .

. ~
The preferred anions are those which are capable of producing a stable diazo salt which is water soluble, e.g., diazos as stabilized salts of zinc chloride, cadmium chloride, stannic chloride, and boron trifluoride have been found to have appropriate water solubility. Accordingly, the hexachlorostannate, tetrachlorozincate and trichlorozincate, trichloro-stannite, hexachlorostannate, tetrafluoroborate, as well as the chloride, bisulfate and sulfate anions, are among the most preferred anions. The water solubility imparted by the anions allow for greater facility in solubilizing the diazo compound in an aqueous reaction medium, and thus for a more practical preparation of the diazonium triflate via precipitation therefrom.
The double salts of the cations can also be formed, and are appropriate for reaction with tri~luoromethane sulfonic acid, or a salt thereof, to yield a diazonium triflate in accordance with the present invention.

,, I i75~1~

The preparation of the diazonium triflates of the present invention can be illustrated by the following equation:

MoSO2cF3+ æ N N ) æ -Il=NO-~-CF3 + MX

The reaction is generally carried out in an aqueous reaction medium to thereby allow recovery of the diazonium triflate product by precipitation from solution. Although the solubility of different diazo triflates will vary, some being less soluble in water than otbers, appropriate steps can be taken, for example, the conditions of temperature, volume, etc.
can be accordingly adjusted, or seeding can be employed, in order to obtain a precipitate in virtually all cases. Due to the appreciable solubility of diazonium triflates in organic solvents, however, reaction in an organic solventl such as hexane or a ketone, would not be practical if one intended to recover the diazonium triflate by precipitation from solution. If an organic reaction medium is employed, however, the triflate could still be recovered there-from by using conventional extraction techniques, e.g., evaporation of the organic solvent.
The reaction in an aqueous medium is carried out by dissolving the diazo salt, f~ N=NX, in the aqueous reaction medium. The trifluoromethyl sulfonic acid or salt, MOS02CF3, is then introduced into the solution. Agitation of the solution can be employed to hasten the dissolution of the trifluoromethyl sulfonic acid. The temperature at which the reaction medium is . . .

~ ~75~

~14-maintained can vary greatly, with the thermal sensitivity of the diazo employed being determinative of a suitable temperature. Generally, however, temperatures ranging from ambient or room temperature to 75C can be employed, with temperatures in the range of about 25C to about 45C being preferred.
Temperatures outside of these ranges) however, can also be employed. The amount of MOSO2CF3 added is preferably slightly in excess of the stoichiometric amount required for reaction with the diazo salt, which is a 1:1 molar ratio.
~he aromatic diazonium cation æ -N= ~- and the trifluoromethyl sulfonate anion ~ SO2CF3 always combine in a 1:1 molar ratio, and thus the exact composition of the reaction product ~-N=NOSO2CF3 is precisely predictable and does not vary from reaction to reaction. This stoichiometry also permits more exacting control of the formulations used in sensitizing diazotype materials.
Precipi~ation of the product diazonium triflate generally occurs without further treatment of the solution. However, in certain instances, precipitation may need to be initiated via adjustment in conditions, e.g., cooling of the aqueous reaction solution, or via seeding the solution. Upon precipitation of the product from solution, the diazonium triflate can be readily recovered via conventional techniques such as filtration.
In situ formation of theldiazonium triflate is also possible. For example, in formulating a sensitizing composition, the composition can be formulated originally with a suitable diazo salt in place of the diazonium triflate. Subseguently, trifluoromethyl sulfonic acid can be added to produce the diazonium triflate in situ. Such technique can ~ 37~

also be employed in the formation of a diazotype light-sensi~ive material, as the original solution or suspension applied to the base or support can be that comprising a suitable dia20 salt capable of forming a diazonium triflate upon reaction with trifluoromethyl sulfonic acid. Accordingly, trifluoromethyl sulfonic acid is added to the treated base or support to form the diazonium triflate in situ.
In accordance with this invention, the following are examples of a number of specific diazonium triflates, same being obtainable by reacting a diazonium salt comprising the cation of said tr:ifla.e and trifluoromethyl sulfonic acid or a salt thereof:

(1) p-N-diethylaminobenzenediazonium 15trifluoromethylsulfonate;
(2) 3-chloro-4-N-diethylaminobenzenediazonium trifluoromethylsulfonate;
(3) o-chlorobenzenediazonium trifluoromethylsulfonate;
20(4) 4 N-diethylamino-2-ethoxybenzenediazonium trifluoromethylsulfonate;
(5) 4-N-diethylamino-2-methylbenzenediazonium trifluoromethylsulfonate;
(6) p-N-dimethylaminobenzenediazonium 25trifluoromethylsulfonate;
(7) 2,5-diisopropoxy-4-morpholinobenzenediazonium trifluoromethylsulfonate;
(8) 4-~3,5-dimethylmorpholino)benzenediazonium trifluoromethylsulfonate;
30(9) o-methoxybenzenediazonium trifluoromethylsulfonate;
~10) 3 chloro-4-N-pyrrolidinobenzenediazonium trifluoromethylsulfonate;

~ 17~

(ll) 3-methyl-4-N-pyrrolidinobenzenediazonium ; trifluoromethylsulfonate;
(12) 3-methoxy-4--N-pyrrolidinobenzenediazonium trifluoromethylsulfonate;
~13) 5-methoxy-2-N-pyrrolidinobenzenediazonium trifluoromethylsulfonate;
~14) 2,4-dimethoxybenzenediazonium trifluoromethylsulfonate;
(15) 2,5-diethoxy-4-(4'-chlorophenoxy)benzenediazonium trifluoromethylsulfonate;
(16) 4-benzyloxybenzenediazonium trifluoromethylsulfonate;
(17~ 2,5-diethoxy-4-N-benzamidobenzenediazonium trifluoromethylsulfonate;
~18) 2-methoxy-5-methyl-4-N-benzamidobenzenediazonium trifluorome~hylsulfonate;
(l9) p-ethoxybenzenediazonium tri~luoromethylsulfonate;
(20) 4-chloronaphthalenediazonium trifluoromethylsulfonate;
(21) 4-pyrrolidinonaphthalenediazonium trifluoromethylsulfonate;
(22) p-chlorobenzenediazonium trifluoromethylsulfonate;
(23) 6-morpholino-3-pyridinediazonium trifluoromethylsulfonate;
(24) 6-dimethylamino-3-pyridinediazonium ~rifluoromethylsulfonate ; (25) 4-N-methanesulfonamido-2,5-dimethoxybenzenediazonium trifluoromethylsulfonate ~26) 4-~2,6-dimethylmorpholino)benzenediazonium trifluoromethylsulfonate;
~27) 4-N-dimethylamino-3-chlorobenzenediazonium trifluoromethylsulfonate;

I 1758~1 ~28) 4-(p-tolylthio)-2,5-dimethoxybenzenediazonium trifluoromethylsulfonate;
(29) 4-N-diethylamino-3-methylbenzenediazonium trifluoromethylsulfonate;
(30) p-N-methylcyc~ohexylamino-3-chlorobenzenediazonium trifluoromethylsulfonate;
(31) 4-N-dimethylamino-3-pyridinediazonium trifluoromethylsulfonate;
(32) 2,5-diethoxy-4-(phenylthio)benzenediazonium trifluoromethyl~ulfonate;
~33) 2,5-dimethoxy-4-morpholinobenzenediazonium trifluoromethylsulfonate;
(34) 4-N~morpholino-2,5-diethcxybenezenediazonium trifluoromethylsulfonate;
(35) 4-N-hexamethyleneiminobenzenediazonium trifluoromethylsulfonate;
~: (36) 4-N-morpholino-5-metboxy-2-(p-tolylthio)benzenediazonium trifluoromethylsulfonate;
(37) 4-N-piperidino-5-methoxy-2-phenoxybenzenediazonium trifluoromethylsulfonate;
(38) 4-N-morpholino-3-methoxybenzenediazonium trifluoromethylsulfonate; and (39) 4-N-benzoylpiperidino-2,5-: 25 diisopropoxybenzenediazonium : trifluoromethylsulfonate.

Other examples of diazonium triflates include those of the structural formulae:

~ 1 75~1 1 Chemical_Structure Chemica1 Name N ~ ~

O-CH3 4-N-methoxycarbonyl-ll amino-2,5-dimethoxy-H3C-O - ~ benzenediaz:onium tri-~ fluoromethylsulfonate ~ C~
H~ ~ 3 1 4-N-acetylamino-~,5-: ~ ~ O-CH3 dimethoxybenzene-: I ll diazonium trifIuoro-C-o ~ methylaulfonate H~ ~S~2CH3 10~ 0-C~13 4~N-methylsulfonyl~
amino-2,5-dimethoxy-C 0- ~ ~ benzenediazonium tri-I fluorosulfonate I 175~

Chemical Structure Chemical Name ,~, N ~
4-N-phenylamino-2-methoxybenzene-~ O-CH diazonium trifluoro-~ 3 methylsulfonate : . N20SO~CF3 ,~
: :

: ~ ~ ~ N ~ 4-N-phenylamino-~ 1 benzenediazonium tri-.~ ~ fluoromethylsulfonate .

~ ; ~ H 4-N-phenylamino--2-.~ 10 trifluoromethyl-- :
, ~ I benzenediazonium tri-~; ~ fluoromethylsulfonate:
,:: 11 1 ~ F3 ~ 1 7~

Chemical Structure Chemical Name _ N ~
¦ 4-N-phenylamino-3-: ~ -CF trifluoromethyl-3 benzenediazonium tri-~ fluoromethylsulfonate '~

N
1 4-N-phenylamino-3-1 chlorobenzene-~1 diazonium trifluoro-/~ methylsulfonate :' :: ~
N20So2CF3 ~ 10 ll ¦ 4-N-benzoylamino-2,5-: H ~ ~ dimethoxybenzene-: ~ / dia20nium trifluoro-i N methylsulfonate CH3 ~

: j ~ . :
, ,' :

~ 1758~

Chemical Structure Chemical Name H\ ~ ~ 4-N-benzoylamino-3-N chlorobenzene-diazonium trifluoro-Cl methylsulfonate 4-N-benæoylamino-3-H ~ methoxybenzene-N diazonium trifluoro-methylsulfonate ~ 4-N-benzoylamino~2-~ ~ ~J chloro-5-methoxy-H ~ ~C ~-' benzenediazonium tri-N fluoromethylsulfonate O-CH
Cl ~

~ ~58~1 Chemical Structure Chemical Name 4~N-acetylamino-2,5-diethoxybenzene~
~ `~ - O-CH2CH3 diazonium tri-l fluoromethylsulfonate CH 3CH2 -O _ ~

;:
~ fH3 : :

4~(p-tolylthio)-2,5-diethoxyben2ene-S diazonium trifluoro-1 methylsulfonate ~)-CH2CH3 ~ : ~ 3 2 ~

:1~ ~ 4-(p tolylthio) 3-chlorobenzene-diazonium trifluoro-methylsulfonate ¢~1 .

, ' , :

.

~ 1758~1 Chemical Structure Chemical Name ¢~
S 4-~p-tolylthio)-3-¦ methoxybenzene-,~ diazonium trifluoro-~0-CH3 methylsulfonate 4-(p-tolylthio)-3-~-: acetylaminobenzene-H diazonium trifluoro-¢ ~ ~ methylsulfonate ~` .

~20S02CF3 carbazole-2-diazonium I I trifluoromethyl-H J sulfonate ~ 175811 Chemical Structure Chemical Name N f 2 2 4--N-ethyl-N-hydroxy-ethylaminobenzene-lr diazonium trifluoro-~20S02CF3 methylsulfonate ;' ~
N 4-N-azacycloheptane-2,5-diethoxybenzene o-CH CH diazonium trifluoro-2 3 methylsulfonate 3CH2-- ~ ~
: N20 2 3 : ~ 3 ; 10 ~ 4-methyl-2-nitro-: ! ~ NO benzenediazonium tri-~ 2 fluoromethylsulfonate , ' 1 ~75811 Chemical Structure Chemical Name p-nitrobenzene-N OSO CF diazonium trifluoro-2 2 3 methylsulfonate Of the specific diazonium triflates named above, the following ~pecies are among those presently preferred:
2,5-diisopropoxy-4-morpholinobenzenediazonium trifluoromethylsulfonate;

; 10 3 -chloro-4-N-pyrrolidinoben2enediazonium : trifluoromethylsulfonate;

3-methyl-4-N-pyrrolidinobenzenediazonium trifluoromethylsulfonate;

3-methoxy-4-N-pyrrolidinobenzenediazonium trifluoromethylsulfonate;

: 2,4-dimethoxybenæenediazonium trifluoromethylsulfonate;

2,5-diethoxy-4-~-benzamidobenzenediazonium trifluorome~hylsulfonate;

4-(2,6-dimethylmorpholino)benzenediazonium trifluoromethylsul~onate;

4-(p-tolylthio)-2,5-dimethoxybenzenediazonium trifluoromethylsulfonate;

'' ~ 175~1~

4-(p-tolylthio~-2,5-diethoxybenzenediazonium trifluoromethylsulfonate;

4-(p-tolylthio)-3-methoxybenzenediazonium trifluoromethylsulfonate;

4-N-azacycloheptane-2,5-diethoxybenzenediazonium trifluoromethylsulfonate;

2,5-diethoxy-4-(phenylthio)benzenediazonium trifluoromethylsulfonate;

~,5-dimethoxy-4-N~morpholinobenzenediazonium trifluoromethylsulfonate;

4-N-morpholino-2,5-diethoxybenzenediazonium trifluoromethylsulfonate;

4-N-hexamethyleneim.inobenzenediazonium ~; 15 trifluoromethylsulfonate;

4-N-morpholino-5-methoxy-2 (p-~olylthio)benzenediazonium trifluoromethyl-sulfonate;

4-~-piperidino-5-methoxy-2-phenoxybenzenediazonium trifluoromethyl-sulfonate;

4-N morpholino-3-methoxybenzenediazonium trifluorome~hylsulfonate; and 4-N-benzoylpiperidino-2,5-diisopropoxybenzenediazonium trifluoromethyl-sulfonate.

~ ~S811 ~27-The diazonium triflates of the present in~ention are light sensitive and undergo the same chemical reactions that characterize aromatic diazo salts. ~ccordingly, diazonium triflates are useful in diazography processes. There are also definite advantages, however, to using diazonium triflates in diazography processes, namely, the ~OS02CF3 anion, in general, imparts a property of lower water solubility to aromatic diazonium cations with which it is combined ; 10 as compared to such conventional diazo stabilized salts of zinc chloride, cadmium chloride, stannic chloride, and the like. This lower water solubility facilitates the economical manufacture of stabilized diazonium triflates in aqueous media~
Moreover, it has also been found that diazonium triflates exhibit a pxoperty of greatly increased organic solvent solubility as compared to conventional diazo salts, including diazonium hexafluorophosphates. This increased solubility in organic solvents such as ketones, alcohols, and the like, which are used for applying diazo formulations to plas~ic layers or carriers in making diazotype materials, aids in the loading of a solvent with the diazo formulation; and, in providing a diazotype material with improved resistance to "blushing". The condition known as "blushing is a result of poor compatibility of a diazosalt with the plastic layer or carrier of a diazotype material, thereby producing a haze on the plastic layer which impairs its transparency and general appearance. The increased solubility of diazonium triflates in the solvent used for applying same to carriers helps to minimize blushing and also provide fox denser images.
Another important advantage of using diazonium triflates, in comparison to known inorganic ~ 1 75~1 ~

fluoride diazo salts such as tetrafluoroborates and hexafluorophosphates, is that triflates do not liberate a corrosive gas, e.g., hydrogen fluoride, during decomposition upon exposure to light as the aforenoted salts. Such gas is very corrosive to glass and can thereby cause rapid deterioration of light sources, which can result in reduced image quality.
Sensitizing compositions comprising diazonium triflates which are useful in diazographic applications can be easily formulated. Diazonium triflates are most adaptable to positive-working diazotype photoreproduction systems by ormulating a sensitizing composition comprising a diazonium triflate as the light sensitive diazonium compound, a diazo coupling component, and an acidic coupling inhibitor as is known in the diazography art, e.g., as disclosed in U.S.
Patent Nos. 3,203,803; 2,694,010; 3,255,011; and, 2,948,613. The coupling component can be any conventional diazo coupler which is normally employed in diazotype materials. Illustrative thereof are:
2,3-dihydroxynaphthalene; 1,8-dihydroxynaphthalene;
phloroglucinol; resorcinol; octylresorcinol; alpha resorcylamid; 3-methyl-1-phenyl-5-pyrazalone;
acetoacetanilide; N-benzylacetoacetamide; 2,3-dihydroxynaphthalene-6-sulfonic acid; 2,5-xylenol; 6,7-dihydroxy-2-naphthalenesulfonic acid; 2,3 naphthalenediol; m-hydroxyphenylurea; 4,4'-thiodiresorcinol; 3,5-dihydroxybenzoic acid; ~-oxynaph-thoic acid monoethanol amide; and mixtures thereof.
The acid coupling inhibitor can also be any conventional and well known inhibitor generally employed in diazotype materials, e.g., citric acid, tartaric acid, boric acid, and the like, In addition to the foregoing materials there can also be included reagents commonly employed in ~ 1'75~

--2g--diazotype photoreproduction materials, as for example, intensifiers such as ammonium sulfate, zinc chloride or nickel sulfates; stabilizing agents such as thiourea, or thiosinamine; accelerators such as l-allyl-3-beta-hydroxyethylthiourea or l-allylthiourea; hygroscopic agents such as gylcol or glycerin; and wetting agents such as saponin, lauryl sulfate, keryl benzene sulfonate or oleyl-N-methyltaurine.
Moreover, there can be included finely divided or colloidal silica or alumina, and/or aqueous dispersions or colloidal solutions of organic film-forming binders, such as colloidal water-soluble polyvinyl alcohol, hydroxyethylcellulose, methyl-cellulose, gelatine or the like, or latex-like dispersions of polyvinyl acetate, polyvinyl chloride, : polyvinyl chloride-acetate, polyvinylidene chloriae, polyacrylonitrile or polymethylmethacrylate.
In order to form a positive-working diazotype - light-sensitive material, the components of the aforedescribed sensitizing formulation are preferably incorporated into a single solution or suspension, and applied in a single coating step to a base or support. The base may be paper~ or a film such as regenerated cellulose, cellulose acetate butyrate, cellulose acetate propionate, silicà/polyvinylbutyral or other plastic films, but most preferably it is a base comprising a polyethylene terephthalate (polyester) film. Other conventional substrates such as textile substrates and nonwovens may also be used.
See generally the U.S. Patent No. 3,976,491 to Desjarlails.
Upon application of the diazonium triflate comprising sensitizing formulation, a diazotype light-; sensitive material comprising a substrate sensitized with said formulation is obtained. Said sensitized ~ ~7S~l~

material can then be subjected to light, i.e., ultraviolet light, to decompose the diazo in the unmasked area, and then same can be developed to allow the undecomposed diazo and coupler to react to form a diazo type.
The diazonium triflates of the present invention are also employable in the Bennett negative-working diazotype photoreproduction system, as disclosed in U.S. Patent ~o. 4,252,884. The sensitizing formulation for such a system comprises a diazonium triflate in the dual role of diazonium compound and light-sensitive acid progenitor, and at least one acid labile enolic, preferably phenolic, blocked coupler adapted to be converted in the presence of acid to an active azo-coupling component~
Preferably, the blocked-coupler has a structural formula selected from the group consisting of R
Y - O - C~R2 R~

RB
~ ~ ~ ~ ~ OR6 ~7 ~ 175~1 R
\

~Rl Y - O - C- ~2' \ R3' Y - O - CH~ - O - CH2CH2 - OCH3 ; and I
A
I
~ Y - O - CH2 - o CH2CH2 - OCH3 ; wherein R1, R2, R3, R4~ Rs~ R6~ ~7~ R8~ Rl ~ R2 and R3~ which may be the ~ame or different~ are selected from the group consisting of alkyl, preferably straight or brancbed chain lower alkyl of from 1 to 8 carbons;
; alkenyl, preferably lower alkenyl of from 2 to about 8 carbons; alkynyl, preferably lower alkynyl of from 2 to about 8 carbon atoms; aryl, preferably aryl having from 6 to about 10 carbons; cycloalkyl, preferably cycloalkyl constituting from 3 to about 8 carbons;
aralkyl, alkaryl, aralkenyl and alkenylaryl, pre~erablY
wherein the alkyl~ aryl and alkenyl groups are as above defined; and, where R5 may also be hydrogen; wherein Y
i5 aryl, e.g., phenyl, naphthyl, anthryl, phenanthryl, and the like; and A is any suitable bridging linkage, e.g., an alkylene group or a direct chemical bond.
Moreover, any two or three of said R substituents may ~ ~758~1 be linked togekher to form a tert-cyclic, bicyclic or heterocyclic structure.
Illustrative of suitable acid labile phenolic blocked-couplers for the Bennett negative-working system are the following: l-naphthyl triphenylmethyl ether; l-methylcyclopentyl l-naphthyl ether; l-butoxy-l-(l-naphthoxy)ethane; t-butyl phenyl ether; 2-(1-naphthoxy)3-methylbutane; l-~l-butoxy)-l-(l-naphthoxy)ethane; l,2-bis(5-t butoxy-l-naphthyl)ethane:
dibenzo~d,f)-2,2-dimethyl-1,3-dioxepine; dibenzo(d,f)-2-methyl-2-phenyl-1,3-dioxepine; dibenzo~d,f)-2,2-diphenyl-1,3-dioxepine; 2,2'-di(2-tetrahydropyranoxy)diphenyl; 2,3-isopropylidenedioxy-naphthalene, t-butyl l-naphthyl ether; l-naphthyl 2-tetrahydropyranyl ether; benzote)-2-phenyl-1,3-dioxin;
l-t-butoxy-5-benzylnaphthalene; t-butyl (4-bromo-1-naphthyl) ether~ dibenzo(d,f)-2-methyl-1,3-dioxepine, methoxyethoxymethyl ~-naphthyl ether; and 3-(methoxyethoxymethoxy)-N-(2-ethylphenyl)-2-naphthalamide.
The enolic-blocked coupler can be used with any effective diazonium triflate. Examples of the most preferred, however, include those diazonium triflates previously listed. It should be appreciated, however, that while the coupler and diazonium salt molecules may bear any one or more substituents which will not interfere with the acid catalyzed unblocking chemistry, at least two sites must be available on the blocked-coupler for any rearrangement and for the subsequent ~ 30 coupling of the unblocked molecule to form an azo dye.
A negative-working diazotype photoreproduction material according to the invention can be conveniently produced by first preparing a solution in pure organic solvents of the two essential components, i.e., a solution of the diazonium triflate ~ ~ 75~

and blocked-coupler. The preferred solvents are generally low molecular weight ketones and alcohols because same, e.g., are typically good solvents for the diazonium triflates. Diazonium triflates, however, are extremely soluble in any organic solvent and thereby the choice need not be limited to ketones and alcohols. In practice, however, it has generally been found advantageous to utilize a mixture of ketone and alcohol solvents.
The blocked-coupler is generally dissolved in the solvent solution with moderate mechanical stirring, then the diazonium triflate is added and dissolved in a similar manner, although the components may be added in reverse order. Conventional additives~ such as intensifiers, accelerators, hydroscopic agents or wetting agents, can also be added to the composition.
One preferred additive is benzotriazole, the incorporation of which into negative-working diazography formulations has been found to improve both the contrast and line acuity of the images derived therefrom when incorporated in an effective amount for same. The amount of benzotriazole has generally been found to be effective when the molar ratio of benzotriazole to diazonium salt in the formulation is in the range from about 1:20 to 1:100.
While the amounts of the respective components formulated are not especially critical, it has been determined for t.he Bennett negative-working system that incorporation of the diazonium tri~late in amounts of up to 7 parts by weight per 100 g of total mix is eminently practicable, preferably not less than 0.5 parts by weight of total ~nix. The blocked-coupler is typically incorporated in a ratio of 0.1 moles per mole diazonium triflate to 2.0 moles per mole diazonium triflate. Preferably, the composition contains a ~ 1~5~11 quantity of approximately 1.0 mole of blocked-coupler per approximately 1.0 mole of diazonium triflate.
Conveniently, the immediately aforesaid diazonium triflate composition or formulation is S applied to any suitable base substrate, e.~.l cellulose acetate butyrate, cellulose acetate propionate~
ethylcellulose, silica/polyvinylbutyral, and preferably to coatings of the aforementioned materials borne by a transparent or opaque polyethylene terephthalate (polyester) film base, by imbibition or bead coating.
It is preferred that approximately 30 grams of mix are laid down per square yard~ This consumption varies according to the specific components utilized, the type and thickness of the polymer, precoating, and the image density desired~ Preferably, the subbed base is overcoated with a layer of cellulose ester, ether, or the like; or the coating can itself comprise a like matrix resin in addition to the solution of the imaging chemicals. A representative film prepared according to the invention would comprise a 0.g2-7 mil bond coated polyester base, overcoated with, e.g., a 0.25 mil matrix resin (for ~xample, cellulose acetate propionate) overcoating including the imaging chemicals. Other suitable substrates include the ; 25 conventional diazo paper bases, textile substrates, nonwovens, etc. See generally the U.S. Patent No.
3,976,491 to Desjarlais.
While the imaging components may all be coated in a single layer, the components may also be in separate layers. For example, the diazonium triflate may be coated onto a matrix coated polyester, a barrier layer applied, then a second matrix layer may be applied to this and the blocked-coupler imbibed into such second layer.

1 ~75811 The resulting light-sensitive diazotype material comprising a support member coated with the diazonium triflate formulation can then be imaged by exposing same to light of a quality and quantity sufficient to photochemically liberate catalytic ~mounts of acid from the diazonium triflate upon decomposition thereof. Reaction of the liberated acid with the blocked-couplers results in an unblocking thereof to yield active azo-couplers. Development of the diazotype material under alkaline conditions produces coupling of the active azo-cvupler with unde-composed diazonium triflate in the light-struck areas to form an azo dye. The diazotype material can be heated prior to or during development to a temperature between about 100 and 210F.
The background areas of the developed film are then preferably cleared in a neutral environment by exposing the same to overall actinic light for a period of about 60 seconds to decompose all the unreacted salt. While this final step is not required, it is generally preferable to include it.
In a further embodiment of the present invention, the diazonium triflates can be employed as latent polymerization initiators in the polymerization of epoxides, cyclic ethers such as oxetanes, cyclic esters such as lactones, and/or mixtures thereof. The process involves forming a mixture of a material polymerizable to higher molecular weights comprising a lactone monomer, an oxetane, a monomeric or prepolymeric epoxide, or mixtures thereof, and a radiation sensitive aromatic diaæonium salt which decomposes upon application of energy thereto to libe-rate a product which thereby initiates the polymerization of said material. Such polymerization processes are described in U.S. Patent Nos. 3,816,279;

~ 1 75~ 1 3,816,~0; 3,816,2~1; 2,S17,845; 3,~17,85~; 3,835,003;
3,9~7,344; 4,054,451; 4,054,452; 4,054,732; ~,056~393;
4,076,536; 4,080,274; and 4,091,194.
Similarly, diazonium triflates decompose upon irradiation thereof to liberate a ~roduct which, when in the presence of cyclic ether or e~ter monomers such as oxetanes, epoxides or lactones, provides cleavage of the carbon-oxygen bond of said ether or ester to thereby initiate growth of a polymeric chain or formation of a cross-linkage. One theoretical mechanism, it being emphasized that same is only theoretical and that applicant does not wish to be bound thereby, is that upon decomposition a triflate aryl ester is formed which then extracts a proton, e.g., from the reaction medium, to form an acid. Said acid is the active agent which then cleaves the carbon-oxygen bond to initiate the polymerization or cross-linkage, and also the agent which reacts with the blocked-coupler of the aforedescribed negative-working diazography system. Thus, as are the photosensitive ; aromatic diazonium salts mentioned in the aforenoted patents, diazonium triflates are applicable as latent polymerization initiators.
A general application of the process for employing diazonium triflates as latent polymerization initiators involves admixing a dia20nium triflate, with or without the use of a suitable solvent, with a polymerizable monomer or mixture of monomers. By a suitable inert solvent is meant one that does not react appreciably with the polymerizable material or the aryldiazonium compound before exposure to actinic radiation. Examples of such solvents include the dimethyl ether of diethylene glycol, anisole, acetonitrile, butyronitrile, toluene, acetone, xylene, methyl ethyl ketone, ethyl ether, cellosolve ether, .

~ 1 75~

1,1,2,2-tetrachloroethane monochlorobenezene, tetrachlor~ethane, o-chlorotoluene, o-dichlorobenzene, trichloroethylene, propylene carbonate, and the like.
Mixtures of these solvents may be employed, par-ticularly if mixtures of epoxides are employed. It is to be understood, however, that the use of solvents is not mandatory.
The amount of photosensitive compound employed in the admixture need not be specifically ascertained but is related to the amount of monomer being polymerized. Quite satisfactory results can be obtained by providing a diazonium triflate in catalytic amounts, preferably an amount by weight of from about 0.5 to about 5% of the catalyst precursor relative to the weight of the polymerizable material provided~
about 2~ or less being amply effective with some of the monomer-catalyst precursor systems.
The polymerizable mixture is thereafter coated on a suitable substrate, such as a metal plate, plastic or paper, and the substrate is exposed to ultraviolet or electron beam radiation. On exposure, the triflate decomposes and provides initiation of the polymerization of the monomer or monomers via cleavage of carbon oxygen bonds~
The source of radiation for carrying out the method of the present invention can be any suitable source, such as the ultraviolet actinic radiation produced from a mercury, xenon, or carbon arc, or the light produced by a cathode ray tube. The only limitation placed on the radiation source used is that it must have an energy level at the irradiated film sufficient to impart to the polymerizable system energy at an intensity high enough to reach the decomposition level of the photosensitive compounds. The wavelength (frequency) range of actinic radiation is generally i 11 7 ~

chosen to obtain sufficient absorption of energy to execute the desired decomposi~ivn.
Such polymerization systems can also be used in imaging systems. For example, a mixture of the mon~mers with epoxides, which may contain a suitable solvent in substantial proportions, is coated on a metal plate, dried if necessary to remove solvent present, and the plate is exposed to ultraviolet light through a mask or negative. The light initiates polymerization which propagates rapidly in the exposed image areas. The resulting polymer in the exposed areas is resistant to many or most solvents and chemicals, while the unexposed areas can be washed with suitable solvents to leave a reversal image of a polymer.
It may be desirable to include in the composition comprising the diazonium triflate and polymerizable material an inert pigment or filler, which may be present in even a major proportion by weight, or small amounts of inert nonvolatile liquids such as mineral oil. Inclusion of such inert ingredients usually makes advisable a proportionate increase in the optimum amount of catalyst precursor used. Nevertheless, the precursors needed rarely exceeds 5% of the entire weight of the composition.
It may further be desirable to include stabilizers or gelation inhibitors for said mixtures of monomers and catalyst. Suitable compounds for such purpose may be sulfoxides such as methyl sulfoxide, ~0 propyl sulfoxide, the l-oxide of tetrahydrothLophene, and the like as disclosed in U.S. Patent No. 3,711,391;
organic amides and ureas such as N,N-dimethylacetamide and 1,1,3l3-tetramethylurea as disclosed in U.S. Patent No. 3,711,390; cyclic amides such as 1-methyl-2-pyrrolidinone, poly(l-vinyl-2-pyrrolidinone), and the ~ ~75811 -3g-like as disclosed in U.5~ Patent No. 3,721,617 and organic nitriles such as acetonitrile as disclosed in U.S. Patent No. 3, 721,616~ When employed as disclosed in said patents, th~ inhibitors are utilized in amounts which may vary from about 0.5 to 5% of the weight of the polymerizable material present in the composition, an amount of inhibitor of less than about 1% by weight of polymerizable material being nearly always sufficient.
In order to further illustrate the present invention, the following specific examples are given, it being understood that same are intended only as illustrative and nowise limitative.

This example illustrates the preparation of the diazonium triflate~ 4-~p-tolylthio)-2,5-~ dimethoxybenzenediazonium trifluoromethylsulfonate.
; ~he representative equation for the reaction is as follows:
~H3 fH3 + F CSO H - - ~ S ~ HCl + 1/2ZnC12 ~ OCH3 ~ ~ OCH3 CH3 ~ CH30 ~
N2 1/2ZnC12 Cl N20S02CF3 ~ ~75811 -40~
41.3 Grams of the 4-~p-tolylthio)-2,5-dimethoxybenzenediazonium zinc chloride double salt and 400 ml of water are placed in a 800 ml beaker. The resulting mixture is stirred and heated to 65C for 30 minutes to yield a hazy solution with suspended solids therein. The solution is clarified of insolubles and the filtrate cooled to about 50-55Co 15 Grams of trifluoromethylsulfonic acid are added dropwise, upon which a yellow copious precipitate forms. The slurry is cooled to about 10C and then filtered to recover the yellow precipitate. The recovered solids are then washed with a small amount of water, and dried via suction. 33.0 Grams of product are obtained.
To the above initial insolubles are added 400 ; ml of water. The solution is heated to 65C, and then clarified of insolubles as before. 5.0 Grams of trifluoromethylsul~onic acid are added to the clarified solution resulting in the formation of a yellow precipitate. The yellow solids are recovered as above to obtain 7.2 grams of purified product, m.p. 106-108C.

30.5 Grams of 3-chloro-4-N-pyrrolidinobenzenediazonium zinc chloride salt are placed in a 500 ml beaker and water added thereto, with stirring, until complete dissolution of the diazo salt occursO The temperature of the resulting solution is `; about 35-40C, with a total of about 300 ml of water having been added. To the solution mixture, which is cloudy, are added two spatulas of filter aid and one spatula of Nuchar. The slurry is then clarified via ~iltration to yield a clear, bright orange solution.
The orange solution is cooled to about 20C
and 15.0 grams of trifluoromethylsulfonic acid is added 1 175~11 thereto at such a rate that a 20C temperature is maintained~ From the first drop of acid, turbidity develops, with precipitation increasing throughout the course of addition. Upon completion of addition, the resulting slurry is stirred for lS minutes at a temperature of about 10-15C, and then filtered to recover a yellow-green precipitate.
The yellow-green solids are washed with a minimal amount of water and dried via suction. The solids are also dried overnight over P2O5. 18.5 Grams of diazonium triflate product are recovered.

In Example 3, the preparation of various diazonium triflates via the following general extraction scheme is illustrated:
To a beaker equipped with magnetic stirring is added 1.0 mole of the respective diazo zinc salt.
The mole of diazo zinc salt is added in a 1:1 (by volume) methylene chloride: water solution containing 13~ of said salt. As the solution is stirred in the beaker, l.OS moles of trifluoromethylsulfonic acid is added dropwise thereto from an addition funnel. The solution is allowed to stir for about five minutesO An amount of the salt equal to 80% of a sa~urated aqueous saline solution is then added to the beaker, and stirring is allowed to continue until the added salt dissolves (approximately 15 minutes). The contents of the beaker are emptied into a separatory funnel, and a split in layers is allowed to occur, with the organic layer being dropped into an Erlenmeyer flask. The organic layer is dried over sodium sulfate, and diluted to three times its volume with hexane. The resulting solution is stirred vigorously and chilled, and then suction filtered to recover diazonium triflate solid.

1 1~5811 The solid is protected from the light while it is washed with hexane and allowed to dry or filtered under vacuum.
In Run 1, a 3-methyl-4-~N-diethyl-amino)benzenediazonium zinc salt is reacted with trifluoromethylsulfonic acid in accordance with the aforedescribed procedure. 3-Methyl-4~(N-diethylamino)benzenediazonium triflate having a melting point of 90-93C is recovered in a 52% yield.
In Run 2, a 2,5-diethoxy~4-(p-~ tolylthio)benzenediazonium zinc salt is reacted with - ~ trifluoromethylsulfonic acid to provide 2,5-diethoxy-4-(p-tolylthio)benzenediazonium triflate, having a melting point of 101 to 104C, in an 85% yield.
In Run 3, a 3-methyl-4-N-pyrrolidinobenzenediazonium zinc salt is reacted in accordance with the aforedescribed scheme. 3-Methyl-4-N-pyrrolidinobenzenediazonium triflate, melting in the range of 119 to 122C, is recovered in a 61% yield.
In Run 4, a 3-chloro-4-N-pyrrolidinobenzenediazonium zinc salt is reacted with trifluoromethylsulfonic acid in arcordance with the aforedescribed process. 3-Chloro-4-N-pyrroli-dinobenzenediazonium triflate, with a melting point range of 90 to 93C, is recovered in a yield of 63%.

~XAMPLE_4 Example 4 illustrates the formulation o~ a positive working, light-sensitive diazotype system and the use thereof in making a light-sensitive diazotype material:

A solution of 2,2'-Dihydroxybiphenyl 1.18 grams 1 175~1~

4-~p-Tolylthio)-2 J 5-die~hoxy-benzenediazonium trifluoromethyl-sulfonate 1.84 grams Methyl alcohol 55 cc ; 5 Acetone 40 cc Methyl cellosolve 5 cc 5-Sulfosalicylic acid .25 gram Zinc chloride ~5 gram Eastman CAP 482.20 12.35 grams is prepared to yield a clear lacquer with a viscosity of approximately 800 centipoise. The lacquer is applied with a suitable coating device to a 4 mil pre-bonded polyester base support and dried 3.5 minutes at 75-80C.
The coated matterial is covered with a printed sheet and exposed to an ultraviolet light source of 400-420 nanometers. The exposed material is passed, without the master, through a standard diazo processor to yield an orange-yellow image reproduction cf the master.
. :

The procedure of Example 4 is followed except that 4-~-pyrrolidino-3-chlorobenæenediazonium trifluoromethylsulfonate is employed as the diazonium triflate. Upon exposure and processing of the light sensitive material, a sepia image reproduction of the master is obtained.

Example 6 illustrates the formulation of a negative-working, light-sensitive, diazotype system and the use thereof in making a light-sensitive diazotype material:

~ ~7S811 A solution of 4-~p-Tolythio)-2,5-dimethoxy-benzenediazon;um trifluoromethylsulfonate 4.30 grams t-butyl naphthyl ether 2.00 grams 5 Acetone 50 cc is coated on a suitably pre-bonded polyester base using an appropriate coating unit and dried at 75-80C for 3.5 minutes. The coating base is exposed through a printed sheet, heated 15 seconds on a SCOTT 24 pre-heater and developed by passing through a Model 6000 dry developer, subsequently cleared of unused diazo from the back for 60 seconds in a SCOTT 716 microcopier. There is obtained a red-purple image with transparent images corresponding to the image of the original master. That is, the image sign has been reversed.

Use of an appropriate 4-N-phenylamino-2-methoxy-benzenediazonium zinc chloride salt in the general pro-cedure of Example 1 or 2 above affords 4-N-phenylamino-2-methoxybenzenediazonium trifluoromethylsulfonate, meltingat 10S-107C.
While the invention has been described in terms of various preferred embodiments, the skilled artisan will appreciate that. various modifications, substitutions, omissions, and changes may be made without departiny from the spirit thereof. ~ccordingly, it is intended that the scope of the present invention be limited solely by the scope of the following claims.

Claims (40)

The embodiments of the invention in which an exclusive property or privilege is claimed are defined as follows:

1. A diazonium trifluoromethane sulfonate having the structural formula:

wherein is the cation of an organic diazonium compound.

2. A compound as defined in claim 1 wherein represents an unsubstituted phenyl, naphthyl, anthryl, phenanthryl, or azaheterocyclic aromatic moiety.

3. A compound as defined in claim 1, wherein , represents a phenyl, naphthyl, anthryl, or phenanthryl moiety having one or more substituents, which may be the same or different, and which are alkyl, alkylamino, dialkylamino, arylamino, aralkylamino, phenoxy, phenyl, phenyl thio ether, morpholino, piperidino, pyrrolidino, hexamethyleneimino, halo, alkoxy, cycloalkyl or piperazino.

4. A compound as defined in claim 2 wherein is the heterocyclic pyridyl moiety.

5. The compound as defined in claim 1 which is:
p-N-diethylaminobenzenediazonium trifluoro-methylsulfonate;
3-chloro-4-N-diethylaminobenzenediazonium trifluoromethylsulfonate;

o-chlorobenzenediazonium trifluoromethyl-sulfonate;

4-N-diethylamino-2-ethoxybenzenediazonium trifluoromethylsulfonate;

4-N-diethylamino-2-methylbenzenediazonium trifluoromethylsulfonate;

p-N-dimethylaminobenzenediazonium trifluoromethylsulfonate 2,5-diisopropoxy-4 morphoIinobenzenediazonium trifluoromethylsulfonate;

4-(2,6-dimethylmorpholino)benzenediazonium trifluoromethylsulfonate;

o-methoxybenzenediazonium trifluoromethylsulfonate;

3-chloro-4-N-pyrrolidinobenzenediazonium trifluoromethylsulfonate;

3-methyl-4-N-pyrrolidinobenzenediazonium trifluoromethylsulfonate;

3-methoxy-4-N-pyrrolidinobenzenediazonium trifluoromethylsulfonate;

5-methoxy-2-N-pyrrolidinobenzenediazonium trifluoromethylsulfonate;

2,4-dimethoxybenzenediazonium trifluoromethyl-sulfonate;

2,5-diethoxy-4-(4'-chlorophenoxy)benzene-diazonium trifluoromethylsulfonate;

4-benzyloxybenzenediazonium trifluoromethyl-sulfonate;

2,5-diethoxy-4-N-benzamidobenzenediazonium trifluoromethylsulfonate;

2-methoxy-5-methyl-4-N-benzamidobenzene-diazonium trifluoromethylsulfonate;

p-ethoxybenzenediazonium trifluoromethyl-sulfonate;

4-chloronaphthalenediazonium trifluoromethyl-sulfonate;

4-pyrrolidinonaphthalenediazonium trifluoro-methylsulfonate;

p-chlorobenzenediazonium trifluoromethyl-sulfonate;

6-morpholino-3-pyridinediazonium trifluoromethylsulfonate;

6-dimethylamino-3-pyridinediazonium trifluoromethylsulfonate;

4-N-dimethylamino-3-pyridinediazonium trifluoromethylsulfonate;

4-N-methoxycarbonylamino-2,5-dimethoxybenzene-diazonium trifluoromethylsulfonate;

4-N-acetylamino-2,5-dimethoxybenzenediazonium trifluoromethylsulfonate;

4-N-methylsulfonylamino-2,5-dimethoxybenzene-diazonium trifluoromethylsulfonate;

4-N-phenylamino-2-methoxybenzenediazonium trifluoromethylsulfonate;

4-N-phenylaminobenzenediazonium trifluoro-methylsulfonate;

4-N-phenylamino-2-trifluoromethyl-benzenediazonium trifluoromethylsulfonate;

4-N-phenylamino-3-trifluoromethylbenzene-diazoniurn trifluoromethylsulfonate;

4-N-phenylamino-3-chlorobenzenediazonium trifluoromethylsulfonate;

4-N-benzoylamino-2,5-dimethoxybenzenediazonium trifluoromethylsulfonate;

4-N-benæoylamino-3-chlorobenzenediazonium trifluoromethylsulfonate;

4-N-benzoylamino-3-methoxybenzenediazonium trifluorornethylsulfonate;

4-N-benzoylamino-2-chloro-5-methoxybenzene-diazonium trifluoromethylsulfonate;

4-N-acetylamino-2,5-diethoxybenzenediazonium trifluoromethylsulfonate;

4-(p-tolylthio)-2,5-diethoxybenzenediazonium trifluoromethylsulfonate;

4-(p-tolylthio)-3-N-acetylaminobenzene-diazonium trifluoromethylsulfonate;

carbazole-2-diazonium trifluoromethyl-sulfonate;

4-N-ethyl-N-hydroxyethylaminobenzenediazonium trifluoromethylsulfonate;

4-N-azacycloheptane-2,5-diethoxybenzene-diazonium trifluoromethylsulfonate;

4-methyl-2-nitrobenzenediazonium trifluoromethylsulfonate;

p-nitrobenzenediazonium trifluoromethyl-sulfonate;

4-N-dimethylamino-3-chlorobenzenediazonium trifluoromethylsulfonate;

4-(p-tolylthio)-2,5-dimethoxybenzenediazonium trifluoromethylsulfonate;

4-N-diethylamino-3-methylbenzenediazonium trifluoromethylsulfonate;

4-(3,5-dimethylmorpholino)benzenediazonium trifluoromethylsulfonate;

4-N-methanesulfonamido-2,5-dimethoxybenzene-diazonium trifluoromethylsulfonate;

p-N-methylcyclohexylamino-3-chlorobenzene-diazonium trifluoromethylsulfonate;

4-(p-tolylthio)-3-chlorobenzenediazonium trifluoromethylsulfonate;

4-(p-tolylthio)-3-methoxybenzenediazonium trifluoromethylsulfonate;

2,5-diethoxy-4-(phenylthio)benzenediazonium trifluoromethylsulfonate;

2,5-dimethoxy-4-morpholinobenzenediazonium trifluoromethylsulfonate;

4-N-morpholino-2,5-diethoxybenezenediazonium trifluoromethylsulfonate;

4-N-hexamethyleneiminobenzenediazonium trifluoromethylsulfonate;

4-N-morpholino-5 methoxy-2-(p-tolylthio)benzenediazonium trifluoromethyl-sulfonate;

4-N-piperidino-5-methoxy-2-phenoxybenzene-diazonium trifluoromethylsulfonate;

4-N-morpholino-3-methoxybenzenediazonium trifluoromethylsulfonate; or 4-N-benzoylpiperidino-2,5-diisopropoxybenzene-Aiazonium trifluoromethylsulfonate.

6. The compound as defined in claim 1 which 4-(p-tolylthio)-2,5-diethoxybenzenediazonium trifluoromethylsulfonate;

4-(p-tolylthio)-3-methoxybenezenediazonium trifluoromethylsulfonate;

4-(p-tolylthio)-2,5-dimethoxybenzenediazonium trifluoromethylsulfonate; or 2,5-diethoxy-4-(phenylthio)benzenediazonium trifluoromethylsulfonate.

7. The compound as defined in claim 1 which 2,5-diisopropoxy-4-morpholinobenzenediazonium trifluoromethylsulfonate;

2,5-dimethoxy-4-N-morpholinobenzenediazonium trifluoromethylsulfonate; or 4-N-morpholino-2,5-diethoxybenzenediazonium trifluoromethylsulfonate.

8. The compound as deined in claim 1 which 4-N-morpholino-5-methoxy-2-(p-tolylthio)benzenediazonium trifluoromethyl-sulfonate;

4-N-morpholino-3-methoxybenzenediazonium trifluoromethylsulfonate; or 4-(2,6-dimethylmorpholino)benzenediazonium trifluoromethylsulfonate.

9. The compound as defined in claim 1 which 3-chloro-4-N-pyrrolidinobenzenediazonium trifluoromethylsulfonate;

3-methyl-4-N-pyrrolidinobenzenediazonium trifluoromethylsulfonate; or 3-methoxy-4-N-pyrrolidinobenzenediazonium trifluoromethylsulfonate.

10. The compound as defined in claim 1 which 4-N-hexamethyleneiminobenzenediazonium trifluoromethylsulfonate; or 4-N-azacycloheptane-2,5-diethoxyben2ene-diazonium trifluoromethylsulfonate.

11. The compound as defined in claim 1 which 4-N-benzoylpiperidino-2,5-diisopropoxybenzene-diazonium trifluoromethylsulfonate; or 4-N-piperidino-5-methoxy-2-phenoxybenzene-diazonium trifluoromethylsulfonate.

12. The compound as defined in claim 1 which is:
2,4-dimethoxybenzenediazonium trifluoromethyl-sulfonate.

13. The compound as defined in claim 1 which is:
2,5-diethoxy-4-N-benzamidobenzenediazonium trifluoromethylsulfonate.

14. A light-sensitive diazography formulation comprising (i) a diazonium trifluoromethane sulfonate as defined in claim 1, (ii) a diazo coupling component, and (iii) an acidic coupling inhibitor.

15. A diazography formulation as defined in claim 14 wherein of said diazonium trifluoromethane sulfonate represents a phenyl, naphthyl, anthryl or phenanthryl moiety having one or more substituents, which may be the same or different, and which are alkyl, alkylamino, dialkylamino, arylamino, aralkyl-amino, phenoxy, phenyl, phenylthio ether, morpholino, piperidino, pyrrolidino, hexamethyleneimino, halo, alkoxy, cycloalkyl or piperazino.

16. A diazography formulation as defined in claim 14 wherein of said diazonium trifluoromethane sulfonate is an azaheterocylic aromatic moiety.

17. A diazotype light sensitive material comprising a support member sensitized with a diazogra-phy formulation as defined in claim 14.

18. A light-sensitive diazography formulation comprising (i) at least one light-sensitive diazonium trifluoromethane sulfonate as defined in claim 1 and (ii) at least one acid labile enolic blocked-coupler adapted to be connected in the presence of acid to an active azo-coupling species.

19. A light-sensitive diazography formulation as defined in claim 18 wherein of said diazonium trifluoromethane sulfonate represents an unsubstituted phenyl, naphthyl, anthryl, phenanthryl or azaheterocylic aromatic moiety.

20. A light-sensitive diazography formulation as defined in claim 18 wherein of said diazonium trifluoromethane sulfonate represents a phenyl, naphthyl, anthryl or phenanthryl moiety having one or more substituents, which may be the same or different, and which are alkyl, alkylamino, dialkylamino, arylamino, aralkylamino, phenoxy, phenyl, phenyl thio ether, morpholino, piperidino, pyrrolidino, hexamethyleneimino, halo, alkoxy, cycloalkyl or piperazino.

21. A light-sensitive diazography formulation as defined in claim 18 wherein said acid labile blocked-coupler has the structural formula:

wherein each R, which may be the same or different, is alkyl, alkenyl, alkynyl, aryl, cycloalkyl, cycloalkenyl, aralkyl, alkaryl, aralkenyl, or alkenylaryl, and Y is aryl.

22. A diazography formulation as defined in claim 18 wherein said acid labile blocked-coupler has the structural formula:

wherein R4 and R5, which may be the same or different, are alkyl, alkenyl, alkynyl, aryl, cycloalkyl, cycloalkenyl, aralkyl, alkaryl, aralkenyl or alkenylaryl, R5 may also be hydrogen, and Y is aryl.

23. A diazography formulation as defined in claim 18 wherein said acid lahile blocked-coupler has the structural formula:

wherein R6, R7 and R8, which may be the same or different, are alkyl, alkenyl, alkynyl, aryl, cycloalkyl, cycloalkenyl, aralkyl, alkaryl, aralkenyl or alkenylaryl, and Y is aryl.

24. A diazography formulation as defined in claim 18 wherein said acid labile blocked-coupler has the structural formula:

wherein each R1, R2 and R3, which may be the same or different, is alkyl, alkenyl, alkynyl, aryl, cycloalkyl, cycloalkenyl, aralkyl, alkaryl, aralkenyl or alkenylaryl, Y is aryl, and A is any bridging linkage.

25. A diazography formulation as defined in claim 18 wherein said acid labile blocked-coupler has the structural formula:

wherein Y is aryl.

26. A diazography formulation as defined in claim 18 wherein said acid labile blocked-coupler has the structural formula:
wherein Y is aryl and A is any bridging linkage.

27. A diazography formulation as defined in claim 18 wherein said acid labile phenolic blocked-coupler is l-naphthyl triphenylmethyl ether; 1-methylcyclopentyl l-naphthyl ether; l-butoxy-l-(l-naphthoxy)ethane; t-butyl phenyl ether; 2-(1-naphthoxy)-3-methylbutane; 1-(-butoxy)-1-(1-naphthoxy)ethane; 1,2-bis(5-t-butoxy-1-naphthyl)ethane;
dibenzo(d,f)-2,2-dimethyl-1,3-dioxepine; dibenzo(d,f)-2-methyl-2-phenyl-1,3-dioxepine; dibenzo(d,f)-2,2-diphenyl-1,3-dioxepine; 2,2'-di(2-tetrahydro-pyranoxy)diphenyl; 2,3-isopropylidenedioxynaphthalene, t-butyl 1-naphthyl ether; 1-naphthyl 2-tetrahydro-pyranyl ether; benzo(e)-2-phenyl-1,3-dioxin; l-t-butoxy-5-benzylnaphthalene; t-butyl (4-bromo-1-naphthyl) ether; dibenzo(d,f)-2-methyl-1,3-dioxepine;
.beta.-methoxyethoxymethyl .alpha.-naphthyl ether; or 3-(methoxyethoxymethoxy)-N-(2-ethylphenyl)-2-naphthalamide.

28. A light-sensitive diazotype photorepro-duction material, comprising a support member sensitized with the diazography formulation as defined in claim 18.

29. A diazotype material as defined in claim 28 wherein the support member is a film substrate.

30. A photopolymerizable composition compris-ing:

(i) a material photopolymerizable to higher molecular weight, said material comprising a lactone monomer, a monomeric or prepolymeric epoxide, an oxetane, or a mixture thereof; and (ii) an effective catalytic amount of a diazonium trifluoromethane sulfonate as defined in claim 1 to initiate the polymerization of said photopolymerizable material upon irradiation thereof.

31. A composition as defined in claim 30 wherein said photopolymerizable material comprises an oxetane.

32. A composition as defined in claim 30 wherein said photopolymerization material comprises a lactone monomer and a monomeric or prepolymeric epoxide.

33. A process of polymerizing a polymerizable material comprising a lactone monomer, monomeric or prepolymeric epoxide, oxetane, or a mixture thereof comprising forming a mixture of said material and a radiation-sensitive diazonium trifluoromethane sulfonate as defined in claim 1, and subsequently exposing the resulting mixture to irradiation of a quantity and quality sufficient to decompose said diazonium trifluoromethane sulfonate and thereby produce a product to initiate the polymerization of said material.

34. A process as defined in claim 33 wherein said photopolymerizable material comprises an oxetane.

35. A process as defined in claim 33 wherein said photopolymerizable material comprises a lactone monomer and a monomeric or prepolymeric epoxide.

36. A positive-working diazography photo-reproduction process comprising imagewise exposing the diazotype material as defined in claim 17 to light of a quality and quantity sufficient to photochemically effect decomposition of the diazonium trifluoromethane sulfonate in the exposed areas, and then developing said diazotype material under alkaline conditions so that coupling occurs between the azo-coupling component and undecomposed diazonium trifluoromethane sulfonate.

37. A negative-working diazography photo-reproduction process comprising imagewise exposing the diazotype material as defined in claim 28 to light of a quality and quantity sufficient to photochemically liberate catalytic amounts of acid therefrom, thus unblocking coupler molecules, and then developing said diazotype material under alkaline conditions such that active azo-coupling species couple with undecomposed diazonium trifluoromethane sulfonate in the light struck areas to form an azo dye.

38. The process as defined in claim 37 wherein the diazotype material is heated prior to or during development to a temperature between about 100 and about 210°F.

39. The process as defined by claim 37, further comprising clearing said developed diazotype material.

40. A photoreproduction process comprising imagewise exposing a support coated with the compo-sition as defined in claim 30 to light of a quality and quantity sufficient to photochemically decompose an amount of diazonium trifluoromethane sulfonate sufficient to thereby initiate polymerization of the polymerizable material in the light struck areas, and then washing the exposed support with a solvent to thereby remove the unpolymerized material in the unexposed areas and leave a reversal image of a polymer in the exposed areas.