Triazolopyridine dyes and thermal transfer of methine dyes

The present invention relates to novel triazolopyridine dyes of the formula I ##STR3## where R.sup.1 is C.sub.1 -C.sub.20 -alkyl, which may be substituted and interrupted by one or more oxygen atoms, or is substituted or unsubstituted phenyl or hydroxyl,
R.sup.2 is a 5- or 6-membered carbocyclic or heterocyclic ring which may be substituted and benzo fused,
R.sup.3 is cyano, carbamoyl, carboxyl or C.sub.1 -C.sub.4 -alkoxycarbonyl,
R.sup.4 is oxygen or a radical of the formula ##STR4##
where L.sup.1 is in each case C.sub.1 -C.sub.4 -alkyl which may be interrupted by 1 or 2 oxygen atoms, and
X is CH or nitrogen,
and to a process for the thermal transfer of methine dyes.
U.S. Pat. No. A-4 769 360 discloses benzoquinoneimine dyes which are derived from p-phenylenediamine derivatives and are said to be suitable for thermal transfer printing. However, it has been found that these dyes have inadequate coloristic properties.
It is an object of the present invention to provide new dyes which are advantageous for the thermal transfer process.
We have found that this object is achieved by the triazolopyridine dyes of the formula I defined at the beginning.
The dyes of the formula I can exist in multiple tautomeric forms which are all encompassed by the claim. For example, compounds where R.sup.4 is oxygen can exist inter alia in the following tautomeric forms: ##STR5##
When R.sup.1 in the formula I is substituted C.sub.1 -C.sub.20 -alkyl, possible substituents are for example phenyl, C.sub.1 -C.sub.4 -alkylphenyl, C.sub.1 -C.sub.4 -alkoxyphenyl, halophenyl, C.sub.1 -C.sub.8 -alkanoyloxy, C.sub.1 -C.sub.20 -alkoxycarbonyl, C.sub.1 -C.sub.20 -alkoxycarbonyloxy, the alkyl chains of the two last-mentioned radicals being optionally interrupted by from 1 to 4 oxygen atoms and/or phenyl- or phenoxy-substituted, halogen, hydroxyl and cyano.
When R.sup.1 in the formula I is alkyl interrupted by oxygen atoms, preference is given to those alkyl radicals which are interrupted by from 1 to 4 oxygen atoms, in particular by 1 or 2 oxygen atoms.
When R.sup.1 in the formula I is substituted phenyl, possible substituents are for example C.sub.1 -C.sub.8 -alkyl, C.sub.1 -C.sub.8 -alkoxy, halogen, in particular chlorine or bromine, and carboxyl.
R.sup.2 can be derived for example from the components of the benzene, indole, quinoline, aminonaphthalene, pyrrole, aminothiazole, benzimidazole, benzothiazole, aminothiophene or diaminopyridine series.
Important radicals R.sup.2 are for example those of the formulae IIa to IIu ##STR6## where n is 0 or 1,
L.sup.2 and L.sup.3 are identical or different and each is independently of the other hydrogen or the abovementioned radical R.sup.1,
R.sup.5 and R.sup.6 are identical or different and each is independently of the other hydrogen, hydroxyl, unsubstituted or phenyl- or C.sub.1 -C.sub.4 -alkylphenyl-substituted C.sub.1 -C.sub.8 -alkyl, unsubstituted or phenyl- or C.sub.1 -C.sub.4 -alkylphenyl-substituted C.sub.1 -C.sub.8 -alkoxy, C.sub.1 -C.sub.8 -alkanoylamino, C.sub.2 -C.sub.8 -alkylsulfonylamino or C.sub.1 -C.sub.8 -monoalkylaminosulfonylamino or -dialkylaminosulfonylamino,
R.sup.7 is hydrogen or methyl,
R.sup.8 is hydrogen, halogen, C.sub.1 -C.sub.8 -alkyl, unsubstituted or C.sub.1 -C.sub.4 -alkyl- or C.sub.1 -C.sub.4 -alkoxy-substituted phenyl, unsubstituted or C.sub.1 -C.sub.4 -alkyl- or C.sub.1 -C.sub.4 -alkoxysubstituted benzyl, cyclohexyl, thienyl, hydroxyl or C.sub.1 -C.sub.8 -monoalkylamino,
R.sup.9 is cyano, carbamoyl, C.sub.1 -C.sub.8 -monoalkylcarbamoyl or -dialkylcarbamoyl or C.sub.1 -C.sub.8 -alkoxycarbonyl, and
R.sup.10 is halogen, hydrogen, C.sub.1 -C.sub.4 -alkyl, C.sub.1 -C.sub.4 -alkoxy, C.sub.1 -C.sub.4 -alkylthio or unsubstituted or C.sub.1 -C.sub.4 -alkylsubstituted phenyl.
Any alkyl appearing in the abovementioned formulae is either straight-chain or branched.
R.sup.1, R.sup.5, R.sup.6, R.sup.8, R.sup.10, L.sup.1 and L.sup.2 are each for example methyl, ethyl, propyl, isopropyl, butyl, isobutyl, secbutyl or tert-butyl.
R.sup.1, R.sup.5, R.sup.6, R.sup.8, L.sup.1 and L.sup.2 may each also be for example pentyl, isopentyl, neopentyl, tert-pentyl, hexyl, 2-methylpentyl, heptyl, 1-ethylpentyl, octyl, 2-ethylhexyl or isooctyl.
R.sup.1 may also be for example nonyl, isononyl, decyl, isodecyl, undecyl, dodecyl, tridecyl, isotridecyl, tetradecyl, pentadecyl, hexadecyl, heptadecyl, octadecyl, nonadecyl, eicosyl (the designations isooctyl, isononyl, isodecyl and isotridecyl are trivial names which are derived from the alcohols obtained by the oxo process--cf. on this point Ullmanns Encyklopadie der technischen Chemie, 4th edition, volume 7, pages 215 to 217, and volume 11, pages 435 and 436).
R.sup.1, L.sup.1 and L.sup.2 may each also be for example 2-methoxyethyl, 2-ethoxyethyl, 2-propoxyethyl, 2-isopropoxyethyl, 2-butoxyethyl, 2- or 3-methoxypropyl, 2- or 3-ethoxypropyl, 2- or 3-propoxypropyl, 2- or 3-butoxypropyl, 2- or 4-methoxybutyl, 2- or 4-ethoxybutyl, 2- or 4-propoxybutyl, 3,6-dioxaheptyl, 3,6-dioxaoctyl, 4,8-dioxanonyl, 3,7-dioxaoctyl, 3,7-dioxanonyl, 4,7-dioxaoctyl, 4,7-dioxanonyl, 2- or 4-butoxybutyl or 4,8-dioxadecyl.
R.sup.1 may also be for example 3,6,9-trioxadecyl, 3,6,9-trioxaundecy1,3,6,9,12-tetraoxatridecy1,3,6,9,12-tetraoxatetradecyl, 2-carboxyethyl, 2-methoxycarbonylethyl, benzyl, 1- or 2-phenylethyl, 3-benzyloxypropyl, phenoxymethyl, 6-phenoxy-4-oxahexyl, 8-phenoxy-4-oxaoctyl, 2-, 3- or 4-chlorophenyl or 2-, 3- or 4-carboxylphenyl.
R.sup.3 and R.sup.9 are each for example methoxycarbonyl, ethoxycarbonyl, propoxycarbonyl, isopropoxycarbonyl, butoxycarbonyl, isobutoxycarbonyl or sec-butoxycarbonyl.
R.sup.9 may also be for example mono- or dimethylcarbamoyl, mono- or diethylcarbamoyl, mono- or dipropylcarbamoyl, mono- or diisopropylcarbamoyl, mono- or dibutylcarbamoyl or N-methyl-N-butylcarbamoyl.
R.sup.5, R.sup.6 and R.sup.10 may each also be for example methoxy, ethoxy, propoxy, isopropoxy, butoxy, isobutoxy or sec-butoxy.
R.sup.10 may also be for example methylthio, ethylthio, propylthio, isopropylthio, butylthio, isobutylthio or sec-butylthio.
R.sup.1, R.sup.8 and R.sup.10 may each also be for example phenyl, 2-, 3- or 4-methylphenyl, 2-, 3- or 4-ethylphenyl, 2-, 3- or 4-propylphenyl, 2-, 3- or 4-isopropylphenyl, 2-, 3- or 4-butylphenyl or 2,4-dimethylphenyl.
R.sup.1 and R.sup.8 may each also be for example 2-, 3- or 4-methoxyphenyl, 2-, 3- or 4-ethoxyphenyl, 2-, 3- or 4-isobutoxyphenyl or 2,4-dimethoxyphenyl.
R.sup.1 may also be for example 2-cyanoethyl, 4-cyanobutyl, 2-hydroxyethyl, 5-hydroxynonyl or a radical of the formula ##STR7##
Preference is given to triazolopyridine dyes of the formula I where R.sup.3 is cyano.
Preference is also given to triazolopyridine dyes of the formula I where R.sup.2 is derived from a component of the benzene, indole, quinoline, aminonaphthalene, pyrrole, aminothiazole, benzimidazole, benzothiazole, aminothiophene or diaminopyridine series.
Preference is also given to triazolopyridine dyes of the formula I where R.sup.1 is C.sub.1 -C.sub.12 -alkyl, which may be substituted by C.sub.1 -C.sub.6 -alkanoyloxy, C.sub.1 -C.sub.8 -alkoxycarbonyl (whose alkyl chains may each be interrupted by 1 or 2 oxygen atoms), phenyl or C.sub.1 -C.sub.4 -alkylphenyl and interrupted by 1 or 2 oxygen atoms.
Particular preference is given to triazolopyridine dyes of the formula I where R.sup.2 is alkyl, alkoxyalkyl, alkanoyloxyalkyl or alkoxycarbonylalkyl, which may each have up to 12 carbon atoms, or is unsubstituted or methyl-substituted benzyl or unsubstituted or methylsubstituted phenyl.
Particular preference is also given to triazolopyridine dyes of the formula I where R.sup.2 is a radical of the abovementioned formula IIa, IIc, IIk, IIl, IIm or IIn, where
L.sup.2 and L.sup.3 are each independently of the other alkyl,
alkoxyalkyl, alkanoyloxyalkyl or alkoxycarbonylalkyl, which may each have up to 12 carbon atoms, or hydrogen, unsubstituted or methyl-substituted benzyl or unsubstituted or methyl-substituted phenyl,
R.sup.5 and R.sup.6 are each independently of the other hydrogen, C.sub.1 -C.sub.4 -alkyl, C.sub.1 -C.sub.4 -alkoxy or C.sub.1 -C.sub.8 -alkanoylamino, and
R.sup.8 is hydrogen, C.sub.1 -C.sub.4 -alkyl, unsubstituted or C.sub.1 -C.sub.4 -alkyl- or C.sub.1 -C.sub.4 -alkoxy-substituted phenyl, benzyl or thienyl.
The dyes of the formula I according to the present invention can be prepared in a conventional manner.
For instance, those triazolopyridine dyes of the formula I where X is CH can be obtained by condensing aldehydes of the formula III
R.sup.2 --CHO (III),
where R.sup.2 is as defined above, with triazolopyridines of the formula IV ##STR8## where R.sup.1, R.sup.3 and R.sup.4 are each as defined above.
Those triazolopyridine dyes of the formula I where X is nitrogen can be obtained for example by condensing the nitroso compounds of the formula V
TI R.sup.2 --NO (V),
where R.sup.2 is as defined above, or by oxidative coupling of the amino compounds of the formula VI
R.sup.2 --NH.sub.2 (VI),
where R.sup.2 is as defined above, with the triazolopyridines IV.
The triazolopyridines of the formula IV are likewise compounds known per se. Their preparation is described for example in earlier German Patent Application P 39 26 770.9.
It is a further object of the present invention to provide a process for the thermal transfer of dyes, a process wherein the dyes used should ideally have no application defects.
In the thermal transfer printing process, a transfer sheet which contains a thermally transferable dye in one or more binders, with or without suitable assistants, on a substrate is heated from the back with an energy source, for example a thermal printing head, in short heating pulses (duration: fractions of a second), as a result of which the dye migrates out of the transfer sheet and diffuses into the surface coating of a receiving medium. The essential advantage of this process is that the amount of dye to be transferred (and hence the color gradation) is easy to control by adjusting the energy supply to the heat source.
In general, color recording is carried out using the three subtractive primaries yellow, magenta and cyan (with or without black). To ensure optimal color recording, the dyes must have the following properties:
ready thermal transferability,
little tendency to migrate within or out of the surface coating of the receiving medium at room temperature,
high thermal and photochemical stability and also resistance to moisture and chemical substances,
suitable hues for subtractive color mixing,
a high molar absorption coefficient,
resistance to crystallization on storage of the transfer sheet,
ready industrial availability.
Experience shows that these requirements are very difficult to meet all at once.
For this reason most of the existing thermal transfer printing dyes fall short of the postulated ideal.
We have found that the object is achieved, and that the transfer of methine dyes by diffusion from a transfer to plastic-coated paper with the aid of an energy source is possible to advantageous effect, on using a transfer on which there is or are situated one or more dyes of the formula I and/or Ia ##STR9## where R.sup.1 is C.sub.1 -C.sub.20 -alkyl, which may be substituted and interrupted by one or more oxygen atoms, or is substituted or unsubstituted phenyl or hydroxyl,
R.sup.2 is a 5- or 6-membered carbocyclic or heterocyclic ring which may be substituted and benzo fused,
R.sup.3 is cyano, carbamoyl, carboxyl or C -C -alkoxycarbonyl,
R.sup.4 is oxygen or a radical of the formula ##STR10## where L.sup.1 is in each case C.sub.1 -C.sub.8 -alkyl which may be interrupted by 1 or 2 oxygen atoms, and
X is CH or nitrogen.
A suitable energy source for the transfer of the dyes of the formula I and/or Ia by diffusion is for example a thermal printing head or a laser. The use of a thermal printing head is preferred.
Preference is given to the process involving the transfer of dyes of the formula I.
Preference is further given to the process involving the transfer of triazolopyridine dyes of the formula I where R.sup.3 is cyano.
Preference is further given to the process involving the transfer of triazolopyridine dyes of the formula I where R.sup.2 is derived from a component of the benzene, indole, quinoline, aminonaphthalene, pyrrole, aminothiazole, benzimidazole, benzothiazole, aminothiophene or diaminopyridine series.
Preference is further given to the process involving the transfer of triazolopyridine dyes of the formula I where R.sup.1 is C.sub.1 -C.sub.12 -alkyl, which may be substituted by C.sub.1 -C.sub.6 -alkanoyloxy, C.sub.1 -C.sub.8 -alkoxycarbonyl (whose alkyl chains may each be interrupted by 1 or 2 oxygen atoms), phenyl or C.sub.1 -C.sub.4 -alkylphenyl and interrupted by 1 or 2 oxygen atoms.
Particular preference is given to the process involving the transfer of triazolopyridine dyes of the formula I where R.sup.1 is alkyl, alkoxyalkyl, alkanoyloxyalkyl or alkoxycarbonylalkyl, which may each have up to 12 carbon atoms, or is unsubstituted or methyl-substituted benzyl or unsubstituted or methyl-substituted phenyl.
Particular preference is further given to the process involving the transfer of triazolopyridine dyes of the formula I where R.sup.2 is a radical of the abovementioned formula IIa, IIc, IIk, IIl, IIm or IIn, where L.sup.2 and L.sup.3 are each independently of the other alkyl, alkoxyalkyl, alkanoyloxyalkyl or alkoxycarbonylalkyl, which may each have up to 12 carbon atoms, or hydrogen, unsubstituted or methyl-substituted benzyl or unsubstituted or methyl-substituted phenyl,
R.sup.5 and R.sup.6 are each independently of the other hydrogen, C.sub.1 -C.sub.4 -alkyl, C.sub.1 -C.sub.4 -alkoxy or C.sub.1 -C.sub.8 -alkanoylamino, and
R.sup.8 is hydrogen, C.sub.1 -C.sub.4 -alkyl, unsubstituted or C.sub.1 -C.sub.4 -alkyl- or C.sub.1 -C.sub.4 -alkoxy-substituted phenyl, benzyl or thienyl.
To prepare the transfer required for the process, the dyes are incorporated into suitable organic solvents, e.g. chlorobenzene, isobutanol, methyl ethyl ketone, methylene chloride, toluene, tetrahydrofuran or a mixture thereof, together with one or more binders and with or without the addition of other auxiliaries, to form a printing ink. It preferably contains the dye in a molecularly dispersed, i.e. dissolved, form. The printing ink is applied to the inert substrate by knife coating and the coating is dried in air. A suitable binder is any resin or polymer material which is soluble in organic solvents and capable of binding the dye to the inert substrate in such a way that it will not rub off. Preference here is given to those binders which, after the printing ink has dried in air, hold the dye in the form of a clear, transparent film without visible crystallization of the dye.
Examples of such binders are cellulose derivatives, eg. methylcellulose, ethylcellulose, ethylhydroxyethylcellulose, hydroxypropylcellulose, cellulose acetate or cellulose acetobutyrate, starch, alginates, allyl resins, vinyl resins, polyvinyl alcohol, polyvinyl acetate, polyvinyl butyrate and polyvinylpyrrolidones. It is also possible to use polymers and copolymers of acrylates or derivatives thereof, such as polyacrylic acid, polymethyl methacrylate or styrene-acrylate copolymers, polyester resins, polyamide resins, polyurethane resins or natural CH resins, such as gum arabic. Other suitable binders are described for example in DE-A-3 524 519.
The preferred binders are ethylcellulose, ethylhydroxyethylcellulose, polyvinyl butyrate and polyvinyl acetate.
The ratio of binder to dye is preferably within the range from 1:1 to 5:1 by weight.
Suitable assistants are for example release agents as described in EP-A-227 092, EP-A-192 435 and the patent applications cited therein and also in particular organic additives which stop the transfer dye from crystallizing in the course of storage or heating of the inked ribbon, for example cholesterol or vanillin.
Inert substrates are for example tissue, blotting or parchment paper or plastics films of high heat stability, for example uncoated or metal-coated polyester, polyamide or polyimide. The inert substrate may additionally be coated on the side facing the energy source with a lubricant, or slipping, layer in order to prevent adhesion of the energy source to the substrate material. Suitable lubricants are described for example in EP-A-216 483 and EP-A-227 095. The thickness of the substrate is in general from 3 to 30 .mu.m, preferably from 5 to 10 .mu.m.
Suitable dye receiver layers are basically all temperature stable plastic layers having an affinity for the dyes to be transferred and preferably glass transition temperatures (T.sup.g) within the range 50.degree. C.<Tg<100.degree. C., e.g. modified polycarbonates and polyesters. Suitable recipes for the receiver layer composition are described in detail for example in EP-A-227 094, EP-A-133 012, EP-A-133 011, EP-A-111 004, JP-A-199 997/1986, JP-A-283 595/1986, JP-A-237 694/1986 and JP-A-127 392/1986.
Transfer is preferably effected, as described above, by means of a thermal printing head which must be heatable to .gtoreq.300.degree. C. for dye transfer to take place within the time interval t: 0<t<15 msec. On heating, the dye migrates out of the transfer sheet and diffuses into the surface coating of the receiving medium.
Compared with the dyes used in existing processes, the novel dyes transferred in the process according to the present invention are in general notable for improved migration properties in the receiving medium at room temperature, readier thermal transferability, readier industrial availability, better resistance to moisture and chemical substances, higher color strength, better solubility, higher thermal and photochemical stability and in particular better purity of hue.
The purity of hue results from the steeper slope of the main absorption band and from the higher transparency in blue and green regions.
The novel dyes give complete coverage of the range from red to turquoise. Of particular interest here are magenta and cyan dyes which, owing to their remarkable brilliance, are suitable as primaries for subtractive color mixing.
Details concerning the preparation are given in the examples, in which percentages are by weight, unless otherwise stated.

The examples which follow illustrate the invention.
Preparation of the Dyes ##STR11##
11 g of N,N-dibutyl-m-toluidine were nitrosated with sodium nitrite at 0.degree. C. to 5.degree. C. in aqueous hydrochloric acid. After 2 hours the mixture was rendered alkaline with 25% strength ammonia at 0.degree.-10.degree. C. and extracted with 150 ml of methylene chloride. The organic phase was then added with stirring to a suspension of 13.6 g of the compound of the formula ##STR12## in acetic anhydride at room temperature. The reaction began immediately to give a slightly exothermic response (32.degree. C.). The mixture was subsequently stirred at room temperature for a further 2 hours, heated to 40.degree. C. and admixed with water to hydrolyse the acetic anhydride. The organic phase was extracted three times with water in a separating funnel and concentrated in a rotary evaporator. The residue was suspended in water, the suspension was neutralized with bicarbonate solution and filtered with suction, and the filter residue was washed until neutral and dried at room temperature.
Yield: 23.3 g=92% of theory
Melting point: 147.degree. C. .lambda..sub.max (THF): 615 nm
R.sub.f : 0.60 (8:2 toluene/ethyl acetate).
Example P1 was also followed to prepare the following dyes by in each case distilling off all the methylene chloride and carrying out the reaction at 120.degree. C.
__________________________________________________________________________ ##STR13## Yield: Melting point: .lambda..sub.max (THF): R.sub.f : 41% of theory .apprxeq.175.degree. C. 614 nm 0.36 (8:2 toluene/ethyl acetate)__________________________________________________________________________
EXAMPLE P3
__________________________________________________________________________ ##STR14## Yield: .lambda..sub.max (THF): R.sub.f : 36% of theory 611 nm 0.38 (8:2 toluene/ethyl acetate)__________________________________________________________________________
EXAMPLE P4
__________________________________________________________________________ ##STR15## Yield: Melting point: .lambda..sub.max (THF): R.sub.f : 29% of theory .apprxeq.180.degree. C. 610 nm 0.29 (8:2 toluene/ethyl acetate)__________________________________________________________________________
EXAMPLE p5
__________________________________________________________________________ ##STR16## Yield: .lambda..sub.max (THF): R.sub.f 30% of theory 626 nm 0.36 (ethyl acetate)__________________________________________________________________________
EXAMPLE P6 ##STR17## 8.3 g of 2-morpholino-5-formylthiazole and 13.6 g of the compound of the formula ##STR18## were dissolved in 100 ml of methylene chloride. After 100 ml of acetic anhydride had been added, the methylene chloride was distilled off and the temperature was increased to 120.degree. C. After cooling to 100.degree. C. with stirring, the target product precipitated. Following addition of 100 ml of methanol, the mixture was stirred overnight and filtered with suction, and the filter residue was washed with methanol and dried.
Yield: 17.1 g=76% of theory
Melting point: >210.degree. C.
.lambda..sub.max (THF): 531 nm
R.sub.f : 0.45 (ethyl acetate)
Example P6 was also followed to synthesize the following dyes:
EXAMPLE P7
__________________________________________________________________________ ##STR19## Yield: Melting point: .lambda..sub.max (THF): R.sub.f : 93% of theory .apprxeq.143.degree. C. 576 nm 0.26 (8:2 (toluene/ethyl acetate)__________________________________________________________________________
EXAMPLE P8
__________________________________________________________________________ ##STR20## Yield: Melting point: .lambda..sub.max (THF): .sub.f : 85% of theory .apprxeq.188.degree. C. 32 nm 0.69 (ethyl acetate)__________________________________________________________________________
EXAMPLE P9
__________________________________________________________________________ ##STR21## Yield: Melting point: Sublimation: .lambda..sub.max (THF): R.sub.f : 64% of theory .apprxeq.205.degree. C. 200.degree. C. 556 nm 0.21 (8:2 ethyl acetate)__________________________________________________________________________
EXAMPLE P10
__________________________________________________________________________ ##STR22## Yield: Melting point: .lambda..sub.max 31% of theory .apprxeq.218.degree. C. 547 nm__________________________________________________________________________
EXAMPLE P11
__________________________________________________________________________ ##STR23## Yield: Melting point: .lambda..sub.max 19% of theory .apprxeq.200.degree. C. 536 nm__________________________________________________________________________ *) Examples P10 and P11 were each carried out using a moist mixture of
EXAMPLE P12
__________________________________________________________________________ ##STR24## Yield: Melting point: Sublimation: .lambda..su b.max (THF): 55% of theory .apprxeq.225.degree. C. 14.degree. C. 528 nm__________________________________________________________________________
Transfer of the Dyes
To be able to test the transfer characteristics of the dyes in a quantitative and simple manner, the heat transfer process was carried out with large hotplates instead of a thermal printing head, the transfer hotplates instead of a thermal printing head, the transfer temperature being varied within the range 70.degree. C.<T<120.degree. C. and the transfer time being set at 2 minutes.
A) General recipe for coating the substrates with dye 1 g of binder were dissolved in 8 ml (8:2 v/v) of toluene/ethanol at from 40.degree. to 50.degree. C. A solution of 0.25 g of dye with or without assistants in 5 ml of tetrahydrofuran was added by stirring. The print paste thus obtained was applied with an 80 .mu.m knife to a sheet of polyester film (thickness: 6-10 .mu.m) and dried with a hairdrier.
B) Testing of thermal transferability
The dyes used were tested in the following manner: The polyester sheet donor containing the dye under test in the coated front was placed face down on a sheet of commercial Hitachi Color Video Print Paper (receiver) and pressed down. Donor/receiver were then wrapped in aluminum foil and heated between two hot plates at different temperatures T (within the temperature range 70.degree. C.<T<120.degree. C.). The amount of dye diffusing into the bright plastic layer of the receiver is proportional to the optical density (=absorbance A). The latter was determined photometrically. If the logarithm of the absorbance A of the colored receiver papers measured within the temperature range from 80.degree. C. to 110.degree. C. is plotted against the corresponding reciprocal of the absolute temperature, the result is a straight line whose slope gives the activation energy .DELTA.E.sub.T for the transfer experiment: ##EQU1##
To complete the characterization, it is additionally possible to infer from the plots the temperature T*[.degree. C] at which the absorbance A of the colored receiver papers attains the value 1.
The dyes listed in the tables which follow were processed according to A), and the resulting dye-coated substrates were tested in respect of their transfer characteristics according to B). The tables list in some instances the thermal transfer parameters T* and .DELTA.E.sub.T, the absorption maxima of the dyes .lambda..sub.max (measured in methylene chloride, unless otherwise stated) and the binders used. The weight ratio of dye:binder is always 1:4. In those cases where an assistant is present, the weight ratio of dye:assistant is 1:0.75.
The following abbreviations apply:
B=binder (EC=ethylcellulose, EHEC=ethylhydroxyethylcellulose, AC=cellulose acetobutyrate, M=mixture of polyvinyl butyrate and ethylcellulose in a weight ratio of 2:1)
A assistant (chol=cholesterol).
TABLE 1__________________________________________________________________________ ##STR25## Ex. Nr. A.sup.1 A.sup.2 A.sup.3 X A.sup.4 .lambda.[nm] B A T* [.degree.C.] ##STR26##__________________________________________________________________________1 CH.sub.3 CH(CH.sub.3).sub.2 H N ##STR27## 610 M -- 108 152 C.sub.2 H.sub.5 C.sub.6 H.sub.13 H N ##STR28## 610 M -- 89 153 C.sub.4 H.sub.9 C.sub.4 H.sub.9 CH.sub.3 N ##STR29## 623 M -- 90 174 C.sub.2 H.sub.5 C.sub.4 H.sub.9 CH.sub.3 N ##STR30## 621 M -- 89 165 C.sub.4 H.sub.9 C.sub.4 H.sub.9 CH.sub.3 N ##STR31## 621 M -- 91 166 C.sub.4 H.sub.9 C.sub.2 H.sub.4 CN H N ##STR32## 590 M -- 111 147 C.sub.2 H.sub.5 C.sub.2 H.sub.5 NHCOCH.sub.3 N ##STR33## 619 M -- 87 198 C.sub.2 H.sub.5 C.sub.2 H.sub.5 NHCOCH.sub.3 N ##STR34## 619 M -- 89 189 C.sub.2 H.sub.5 C.sub.4 H.sub.9 NHCOCH.sub.3 N C.sub.3 H.sub.6 OC.sub.2 H.sub.4 OC.sub.4 H.sub.9 620 EHEC -- 93 1810 C.sub.4 H.sub.9 C.sub.4 H.sub.9 NHCOCH.sub.3 N ##STR35## 623 M -- 110 1511 C.sub.2 H.sub.5 C.sub.2 H.sub.5 NHSO.sub.2 N(CH.sub.3).sub.2 N ##STR36## 618 M -- 90 1412 C.sub.2 H.sub.5 C.sub.2 H.sub.5 H CH ##STR37## 559 M -- 89 1113 CH.sub.3 CH.sub.3 H CH ##STR38## 554 M -- 112 1614 C.sub.4 H.sub.9 C.sub.2 H.sub.5 OCH.sub.3 CH ##STR39## AC Chol 87 1315 C.sub.4 H.sub.9 C.sub.2 H.sub.5 OCH.sub.3 N C.sub.4 H.sub.8 OC.sub.3 H.sub.7 EC -- 92 16__________________________________________________________________________
TABLE 2__________________________________________________________________________ ##STR40## Ex. Nr. A.sup.1 A.sup.2 A.sup.3 X .lambda.[nm] B A T* [.degree.C.] ##STR41##__________________________________________________________________________16 C.sub.2 H.sub.5 C.sub.4 H.sub.9 C.sub.6 H.sub.5 N 612 M -- 86 1617 C.sub.2 H.sub.5 C.sub.2 H.sub.5 C.sub.6 H.sub.5 N 615 M -- 82 1618 CH(CH.sub.3).sub.2 CH(CH.sub.3).sub.2 C.sub.6 H.sub.5 N 617 M -- 90 1719 C.sub.2 H.sub.5 C.sub.2 H.sub.5 ##STR42## N 624 M -- 90 1320 C.sub.2 H.sub.5 C.sub.2 H.sub.5 ##STR43## N 621 M -- 92 1221 C.sub.2 H.sub.5 C.sub.4 H.sub.9 ##STR44## N 612 M -- 84 1722 C.sub.2 H.sub.5 C.sub.4 H.sub.9 ##STR45## N 611 M -- 85 1623 C.sub.2 H.sub.5 C.sub.2 H.sub.5 C.sub.6 H.sub.5 CH 560 M -- 85 1224 C.sub.2 H.sub.5 C.sub.2 H.sub.5 Thien-2-yl CH 579 M -- 90 1625 Benzyl CH.sub.3 H CH 537 M -- 88 826 C.sub.4 H.sub.9 C.sub.2 H.sub.5 C.sub.6 H.sub.5 CH 561 M -- 90 1227 C.sub.2 H.sub.5 C.sub.2 H.sub.5 ##STR46## CH 566 M -- 109 10__________________________________________________________________________
TABLE 3__________________________________________________________________________ ##STR47## Ex. No. A.sup.1 A.sup.3 X A.sup.4 .lambda.[nm] B A T* [.degree.C.] ##STR48##__________________________________________________________________________28 C.sub.2 H.sub.4 OC.sub.4 H.sub.9 H N ##STR49## 631 M -- 110 2429 C.sub.6 H.sub.13 H N ##STR50## 636 EC Chol 107 2230 C.sub.3 H.sub.7 CH.sub.3 N C.sub.3 H.sub.6 OC.sub.2 H.sub.4 OC.sub.4 H.sub.9 640 EC -- 100 1631 C.sub.2 H.sub.5 H CH ##STR51## -- M -- 98 1532 C.sub.2 H.sub.4 OC.sub.4 H.sub.9 CH.sub.3 CH ##STR52## -- EC -- 100 1633 H NHCOCH.sub.3 N ##STR53## 616 M -- 98 14__________________________________________________________________________
TABLE 4__________________________________________________________________________ ##STR54## Ex. No. A.sup.1 A.sup.2 A.sup.3 X .lambda.[nm] B A T* [.degree.C.] ##STR55##__________________________________________________________________________34 H CH(CH.sub.3).sub.2 CH(CH.sub.3).sub.2 N 608 N -- 101 1635 C.sub.2 H.sub.5 C.sub.3 H.sub.6 OCH.sub. 3 C.sub.3 H.sub.6 OCH.sub.3 N 619 N -- 94 17__________________________________________________________________________
TABLE 5______________________________________ ##STR56## No.Ex. Y A.sup.3 X .lambda.[nm] B A [.degree.C.]T* ##STR57##______________________________________36 CH.sub.2 C.sub.6 H.sub.5 N 616 M -- 90 1437 O C.sub.6 H.sub. 5 N 612 M -- 92 1538 O H CH 537 M -- 87 13______________________________________
TABLE 6__________________________________________________________________________ ##STR58## Ex. No. A.sup.1 A.sup.2 A.sup.3 X A.sup.4 .lambda.[nm] B A T* [.degree.C.] ##STR59##__________________________________________________________________________39 C.sub.2 H.sub.5 C.sub.2 H.sub.5 NHCOCH.sub.3 N ##STR60## 593 EC -- 129 1540 C.sub.2 H.sub.5 C.sub.2 H.sub.5 NHCOCH.sub.3 N ##STR61## 593 EC -- 121 1341 C.sub.2 H.sub.5 C.sub.2 H.sub.5 OCH.sub.3 N ##STR62## 570 EC -- 127 1042 C.sub.2 H.sub.5 C.sub.2 H.sub.5 OCH.sub.3 N ##STR63## 570 EC -- 117 1043 C.sub.2 H.sub.5 C.sub.2 H.sub.5 H CH C.sub.6 H.sub.13 528 M -- 78 14__________________________________________________________________________
TABLE 7__________________________________________________________________________ ##STR64## No.Ex. A.sup.1 A.sup.2 A.sup.3 X A.sup.4 .lambda.[nm] B A [.degree.C.]T* ##STR65##__________________________________________________________________________44 C.sub.3 H.sub.7 CH.sub.2 (C.sub.2 H.sub.4 O).sub.2 CH.sub.3 2-Thienyl N C.sub.2 H.sub.4 OCH.sub.3 626* EC -- 100 1445 C.sub.2 H.sub.5 (C.sub.2 H.sub. 4 O).sub.2 C.sub.2 H.sub.5 C.sub.6 H.sub.5 N C.sub.3 H.sub.6 OC.sub.2 H.sub.5 584* M -- 94 1346 C.sub.3 H.sub.7 CH.sub.2 (C.sub.2 H.sub.4 O).sub.2 CH.sub.3 2-Thienyl N C.sub.3 H.sub.6 OCH.sub.3 624* M -- 98 1247 C.sub.2 H.sub.5 (C.sub.2 H.sub.4 O).sub.3 C.sub.2 H.sub.5 C.sub.6 H.sub.5 N C.sub.2 H.sub.4 OCH.sub.3 584* EC -- 94 1448 C.sub.2 H.sub.5 (C.sub.2 H.sub.4 O).sub.3 C.sub.2 H.sub.5 C.sub.6 H.sub.5 N C.sub.3 H.sub.6 OCH.sub.3 584* M -- 96 1349 C.sub.2 H.sub.5 CH.sub.2 (C.sub.2 H.sub.4 O).sub.2 CH.sub.3 C.sub.6 H.sub.5 N C.sub.2 H.sub.4 OCH.sub.3 585* M -- 97 1450 C.sub.2 H.sub.5 C.sub.2 H.sub.5 C.sub.6 H.sub.5 CH C.sub.2 H.sub.4 OCH.sub.3 534 M -- 91 1351 C.sub.2 H.sub.5 C.sub.2 H.sub.5 ##STR66## CH C.sub. 6 H.sub.13 537 M -- 84 1852 C.sub.2 H.sub.5 C.sub.2 H.sub.5 Thien-2-y CH C.sub.6 H.sub.13 551 M -- 88 19__________________________________________________________________________ *.lambda..sub.max was measured in THF
TABLE 8______________________________________ ##STR67## No.Ex. .lambda.[nm] B A [.degree.C.]T* ##STR68##______________________________________53 590 M -- 99 12______________________________________
Similar results are obtained with the dyes listed in Table 9. (The roman numerals under D refer to the abovementioned radicals of the formula II).
TABLE 9__________________________________________________________________________ ##STR69##Ex.-No. D X L.sup.2 R.sup.1 L.sup.3 R.sup.5 R.sup.6 Hue__________________________________________________________________________54 IIa CH C.sub.4 H.sub.9 ##STR70## C.sub.2 H.sub.5 H H Magenta violet55 IIa CH C.sub.2 H.sub.5 C.sub.2 H.sub.5 C.sub.3 H.sub.7 H H Magenta violet56 IIa CH C.sub.2 H.sub.4 CO.sub.2 C.sub.2 H.sub.5 C.sub.4 H.sub.8 OCH.sub.3 C.sub.2 H.sub.5 H H Magenta57 IIa CH C.sub.2 H.sub.5 C.sub.3 H.sub.6 OC.sub.4 H.sub.9 C.sub.2 H.sub.5 H CH.sub.3 Magenta violet58 IIa CH CH(CH.sub.3).sub.2 ##STR71## CH(CH.sub.3).sub.2 H OCH.sub.3 Magenta violet59 IIa CH C.sub.4 H.sub.9 ##STR72## C.sub.2 H.sub.5 H CH.sub.3 Magenta violet60 IIa CH C.sub.4 H.sub.9 C.sub.7 H.sub.15 C.sub.2 H.sub.5 H NHCOCH.sub.3 Magenta violet61 IIa CH C.sub.3 H.sub.7 (CH.sub.2).sub.2 CO.sub.2 C.sub.4 H.sub.9 C.sub.3 H.sub.6 OCH.sub.3 H H Magenta62 IIa N C.sub.4 H.sub.9 (CH.sub.2).sub.2 CO.sub.2 C.sub.4 H.sub.9 C.sub.4 H.sub.9 H H Cyan63 IIa N C.sub.2 H.sub.5 C.sub.3 H.sub.6 OC.sub.2 H.sub.4 OCH.sub.3 C.sub.2 H.sub.5 H C.sub.2 H.sub.5 Cyan64 IIa N C.sub.2 H.sub.5 ##STR73## C.sub.3 H.sub.7 H CH.sub.3 Cyan65 IIa N CH(CH.sub.3).sub.2 (CH.sub.2).sub.4 OC.sub.3 H.sub.7 C.sub.2 H.sub.5 H C.sub.2 H.sub.5 Cyan66 IIa N C.sub.4 H.sub.9 ##STR74## C.sub.2 H.sub.5 H NHCOCH.sub.3 Cyan67 IIa N C.sub.3 H.sub.7 ##STR75## C.sub.2 H.sub.5 H NHSO.sub.2 C.sub.4 H.sub.9 Cyan68 IIa N C.sub.2 H.sub.5 C.sub.2 H.sub.4 OC.sub.4 H.sub.9 C.sub.7 H.sub.15 H NHSO.sub.2 C.sub.2 H.sub.5 Cyan69 IIa N H ##STR76## C.sub.4 H.sub.9 OCH.sub.3 CH.sub.3 Cyan70 IIa N C.sub.2 H.sub.4 CN (CH.sub.2).sub.2 OC.sub.6 H.sub.13 C.sub.4 H.sub.9 H CH.sub.3 Cyan71 IIa N H ##STR77## C.sub.5 H.sub.11 OC.sub.2 H.sub.5 CH.sub.3 Cyan72 IIb CH C.sub.2 H.sub.5 ##STR78## -- -- H Magenta violet__________________________________________________________________________Ex.-No. D X L.sup.2 R.sup.1 L.sup.4 R.sup.6 R.sup.5 Hue__________________________________________________________________________73 IIb CH C.sub.4 H.sub.9 (CH.sub.2).sub.4 OC.sub.4 H.sub.9 -- -- H violet74 IIb N C.sub.2 H.sub.5 ##STR79## -- -- H Cyan75 IIc CH C.sub.4 H.sub.9 (C.sub.2 H.sub.4 O).sub.2 C.sub.4 H.sub.9 -- -- H Magenta violet76 IIc CH C.sub.3 H.sub.6 OC.sub.4 H.sub.9 ##STR80## -- -- H Magenta violet77 IIc CH C.sub.2 H.sub.5 (C.sub.2 H.sub.4 O).sub.2 C.sub.4 H.sub.9 -- -- H Magenta violet78 IIc CH C.sub.2 H.sub.5 C.sub. 3 H.sub.6 OC.sub.2 H.sub.4 OC.sub.6 H.sub.5 -- -- CH.sub.3 violet79 IIc CH C.sub.4 H.sub.9 (CH.sub.2).sub.2 CO.sub.2 C.sub.5 H.sub.11 -- -- OCH.sub.3 violet80 IIc CH C.sub.2 H.sub.5 (CH.sub.2).sub.2 OC.sub.5 H.sub.11 -- -- C.sub.2 H.sub.5 violet81 IIc CH C.sub.2 H.sub.4 CN (CH.sub.2).sub.2 OC.sub.5 H.sub.11 -- -- H Magenta82 IIc CH C.sub.2 H.sub.4 OH (C.sub.2 H.sub.4 O).sub.2 C.sub.4 H.sub.9 -- -- CH.sub.3 Magenta83 IIc CH C.sub.2 H.sub.4 CO.sub.2 C.sub.2 H.sub.5 (C.sub.2 H.sub.4 O).sub.2 C.sub.4 H.sub.9 -- -- H Magenta84 IIc N (C.sub.2 H.sub.4 O).sub.2 C.sub.4 H.sub.9 ##STR81## -- -- H Cyan85 IIc N C.sub.2 H.sub.5 (CH.sub.2).sub.4 OC.sub.3 H.sub.6 OC.sub.2 H.sub.5 -- -- CH.sub.3 Cyan Turquoise86 IIc N C.sub.4 H.sub.9 CH.sub.3 -- -- H Cyan87 IIc N H C.sub.4 H.sub.8 OC.sub.3 H.sub.6 OC.sub.4 H.sub.9 -- -- CH.sub.3 Cyan88 IIc N C.sub.3 H.sub.7 ##STR82## -- -- NHCOCH.sub.3 Cyan Turquoise89 IIc N C.sub.2 H.sub.4 CN C.sub.3 H.sub.6 OC.sub.2 H.sub.4 OC.sub.4 H.sub.9 -- -- CH.sub.3 Cyan90 IIc N C.sub.3 H.sub.6 (C.sub.2 H.sub.4 O).sub.2 C.sub.4 H.sub.9 -- -- H Cyan91 IIc N C.sub.2 H.sub.5 C.sub.2 H.sub.4 CO.sub.2 C.sub.7 H.sub.15 -- -- CH.sub.3 Cyan Turquoise92 IIc N C.sub.2 H.sub.4 OH C.sub.3 H.sub.6 OC.sub.3 H.sub.6 OC.sub.2 H.sub.5 -- -- H Cyan93 IId CH -- ##STR83## -- H H Yellow94 IId CH -- C.sub.3 H.sub.6 OC.sub.4 H.sub.9 -- m-CH.sub.3 OC.sub.2 H.sub.5 Yellow95 IId CH -- ##STR84## -- m-CO.sub.2 C.sub.6 H.sub.13 H Yellow__________________________________________________________________________ ##STR85##Ex.-No. D X L.sup.2 R.sup.1 L.sup.3 R.sup.6 R.sup.5 Hue__________________________________________________________________________96 IIe CH C.sub.3 H.sub.6 OC.sub.4 H.sub.9 ##STR86## -- -- CH.sub.3 Magenta violet97 IIe N C.sub.3 H.sub.7 ##STR87## -- -- H Cyan Turquoise98 IIe N ##STR88## ##STR89## -- -- CH.sub.3 Turquoise99 IIg CH -- ##STR90## -- -- H Magenta violet100 IIg CH -- C.sub.3 H.sub.6 OC.sub.2 H.sub.4 OC.sub.6 H.sub.5 -- -- CH.sub.3 violet101 IIg N -- C.sub.3 H.sub.6 OC.sub.2 H.sub.4 OC.sub.4 H.sub.9 -- -- H Cyan102 IIg N -- ##STR91## -- -- CH.sub.3 Cyan Turquiose103 IIg N -- C.sub.3 H.sub.6 OC.sub.3 H.sub.7 -- -- NHCOCH.sub.3 Cyan Turquiose__________________________________________________________________________
TABLE 10__________________________________________________________________________ ##STR92## Ex.- No. A.sup.1 A.sup.2 A.sup.3 X A.sup.4 .lambda.[mm] B A T*[.degree.C.] ##STR93##__________________________________________________________________________104 CH(CH.sub.3).sub.2 C.sub.2 H.sub.5 CH.sub.3 N ##STR94## 621 EHEC -- 96 12105 C.sub.3 H.sub.7 C.sub.2 H.sub.5 CH.sub.3 N ##STR95## 621 EHEC -- 111 14106 C.sub.4 H.sub.9 C.sub.4 H.sub.9 NHCOC.sub.3 H.sub.7 N ##STR96## 625 EHEC -- 105 10107 ##STR97## C.sub.2 H.sub.5 H CH ##STR98## 555 EHEC -- 100 9108 C.sub.2 H.sub.4 OCOCH.sub.2 OCH.sub.3 C.sub.2 H.sub.5 H N ##STR99## 601 M -- 87 10109 C.sub.2 H.sub.4 Cl C.sub.2 H.sub.5 H N ##STR100## 595 M -- 84 9110 C.sub.2 H.sub.5 C.sub.2 H.sub.5 NHCO.sub.2 C.sub.2 H.sub.4 OC.sub.2 H.sub.5 N ##STR101## 616 M -- 76 10111 ##STR102## C.sub.2 H.sub.5 H N ##STR103## 604 M -- 76 8112 C.sub.2 H.sub.4 OCOCH.sub.3 C.sub.2 H.sub.5 H N ##STR104## 604 EHEC -- 104 10113 ##STR105## C.sub.2 H.sub.5 CH.sub.3 N ##STR106## 618 M -- 78 10114 C.sub.4 H.sub.9 C.sub.2 H.sub.5 CH.sub.3 N ##STR107## 618 M -- 94 11115 C.sub.4 H.sub.9 C.sub.4 H.sub.9 CH.sub.3 N ##STR108## 621 M -- 94 11116 ##STR109## C.sub.2 H.sub.5 CH.sub.3 N ##STR110## 618 M -- 80 8117 C.sub.4 H.sub.9 C.sub.4 H.sub.9 H N C.sub.3 H.sub.7 616 M -- 73 7118 C.sub.2 H.sub.5 C.sub.2 H.sub.5 OCH(CH.sub.3).sub.2 N ##STR111## 601 M -- 82 9119 CH.sub.3 CH.sub.3 H CH ##STR112## 554 M -- 112 16120 C.sub.2 H.sub.4 OC.sub.4 H.sub.9 C.sub.2 H.sub.5 H N ##STR113## 615 M -- 109 11121 C.sub.2 H.sub.4 CN C.sub.4 H.sub.9 H N ##STR114## 590 M -- 111 13122 C.sub.4 H.sub.9 C.sub.4 H.sub.9 H N ##STR115## 620 M -- 110 12123 C.sub.4 H.sub.9 C.sub.2 H.sub.5 CH.sub.3 N ##STR116## 621 M -- 117 16124 C.sub.4 H.sub.9 C.sub.2 H.sub.5 CH.sub.3 N CH.sub.3 619 M -- 85 9125 C.sub.4 H.sub.9 C.sub.4 H.sub.9 CH.sub.3 N C.sub.2 H.sub.5 619 M -- 83 10126 C.sub.4 H.sub.9 C.sub.2 H.sub.5 CH.sub.3 N C.sub.2 H.sub.5 621 M -- 119 13127 C.sub.4 H.sub.9 C.sub.4 H.sub.9 CH.sub.3 N ##STR117## 625 M -- 88 12128 C.sub.4 H.sub.9 C.sub.4 H.sub.9 CH.sub.3 N CH.sub.3 621 M -- 108 10129 C.sub.4 H.sub.9 CH.sub.3 H N ##STR118## 607 M -- 82 9130 C.sub.2 H.sub.5 C.sub.2 H.sub.5 CH.sub.3 N ##STR119## 615 M -- 83 11131 (CH.sub.2).sub.2 CH(CH.sub.3).sub.2 C.sub.2 H.sub.5 CH.sub.3 N ##STR120## 620 EHEC -- 92 13132 C.sub.2 H.sub.4 CH(CH.sub.3).sub.2 C.sub.2 H.sub.5 CH.sub.3 N C(CH.sub.3).sub.3 621 M -- 102 8133 CH.sub.2 CH(CH.sub.3).sub.2 C.sub.4 H.sub.9 H N C(CH.sub.3).sub.3 615 M -- 83 11134 C.sub.4 H.sub.9 C.sub.4 H.sub.9 OCH.sub.3 N ##STR121## 603 M -- 98 6135 C.sub.2 H.sub.4 OCONHC.sub.4 H.sub.9 C.sub.2 H.sub.5 H N ##STR122## 596 M -- 97 16136 C.sub.2 H.sub.5 C.sub.2 H.sub.5 H N ##STR123## 608 M -- 97 14137 C.sub.2 H.sub.5 C.sub.2 H.sub.5 NHCOCH.sub.2 OCH.sub.3 N ##STR124## 622 M -- 93 8138 C.sub.2 H.sub.4 OC.sub.2 H.sub.5 C.sub.2 H.sub.5 NHCOCH.sub.3 N ##STR125## 623 M -- 88 8139 C.sub.2 H.sub.5 C.sub.2 H.sub.5 ##STR126## N ##STR127## 624 M -- 81 8140 C.sub.2 H.sub.4 O.sub.2 CCH.sub.3 C.sub.2 H.sub.4 O.sub.2 CH.sub.3 NHCOCH.sub.2 OCH.sub.3 N ##STR128## 615 M -- 82 8141 C.sub.2 H.sub.4 O.sub.2 CC.sub.5 C.sub.2 H.sub.4 O.sub.2 CC.sub.2 H.sub.5 NHCOC.sub.2 H.sub.5 N ##STR129## 616 M -- 83 10__________________________________________________________________________
TABLE 11__________________________________________________________________________ ##STR130## No.Ex. A.sup.1 A.sup.2 A.sup.3 X A.sup.4 .lambda.[mm] B A T*[.degree.C.] ##STR131##__________________________________________________________________________142 C.sub.2 H.sub.5 C.sub.2 H.sub.5 ##STR132## CH ##STR133## 563 M -- 155 3143 C.sub.2 H.sub.5 C.sub.2 H.sub.5 ##STR134## N ##STR135## 623 M -- 101 10__________________________________________________________________________
TABLE 12__________________________________________________________________________ ##STR136##Ex.No. D X L.sup.2 R.sup.1 L.sup.3 Y R.sup.5 R.sup.6 R.sup.8 .lambda..sub.max (nm)__________________________________________________________________________144 IIa N CH.sub.3 ##STR137## CH.sub.3 CO.sub.2 C.sub.4 H.sub.9 H H -- 680145 IIa CH C.sub.2 H.sub.5 ##STR138## C.sub.4 H.sub.9 CO.sub.2 C.sub.4 H.sub.9 H H -- 638146 IIk CH C.sub.2 H.sub.5 ##STR139## C.sub.2 H.sub.5 CN -- -- C.sub.6 H.sub.5 636147 IIk CH C.sub.2 H.sub.5 ##STR140## C.sub.2 H.sub.5 CN -- -- ##STR141## 620__________________________________________________________________________

Number	Date	Country
0111004	Jun 1984	EPX
0133011	Feb 1985	EPX
0133012	Feb 1985	EPX
0192435	Aug 1986	EPX
0216483	Apr 1987	EPX
0227092	Jul 1987	EPX
0227094	Jul 1987	EPX
0227095	Jul 1987	EPX
0245860	Nov 1987	EPX
3524519	Jan 1986	DEX
2161824A	Jan 1986	GBX

Triazolopyridine dyes and thermal transfer of methine dyes

Information

Patent Number

Date Filed

Date Issued

Inventors

Original Assignees

Examiners

Agents

CPC

US Classifications

Field of Search

US

International Classifications

Abstract

Description

Claims

Priority Claims (1)

US Referenced Citations (1)

Foreign Referenced Citations (11)