US 4,889,932 AGrant
Stabilized Leuco Phenazine Dyes and Their Use in an Imaging System
Issue Date:1989-12-26
•5 Claims
Abstract
3,7-Diamino phenazine leuco dyes stabilized in the 10-position with acyl substituents, said acyl substituents being themselves substituted with electron withdrawing groups. The structure of the reduced form of the dye can be represented by the general formula: ##STR1## wherein R.sup.1 represents a member selected from the group consisting of aryl groups having up to 14 carbon atoms and containing from 1 to 5 electrons withdrawing substituents, alkyl groups having up to 4 carbon atoms and containing one or more electron withdrawing groups, certain electron withdrawing groups containing a ##STR2## moiety, and certain electron withdrawing groups containing a --NH-- moiety. These dyes are suitable for use in thermographic imaging systems wherein the leuco dye is in a composition containing a nitrate salt.
Metadata
Assignee
- Minnesota Mining and Manufacturing Company
Inventor
- Alan G. Miller
Application Information
Application Number:US 1532642
Filing Date:1988-02-08
Priority Date:1984-10-01
Art Unit:122
Classifications
IPC:
C07D24146B41M 526B41M 512C09B 1702
Field of Search:
544348
Patent Drawings
This patent does not have any drawings.
Description
Example I
This example demonstrates the preparation of 5,10-dihydro-5-phenyl-10-(4-phenylsulfonylbenzoyl)-3,7-di (N,N-diethylamino)phenazine (leuco dye no. 9 of Table I).
Into a 1-liter, 3-neck round-bottom flask equipped with a mechanical stirrer, pH electrode, and an argon inlet and outlet, was added 10.0 g (0.023 M) tetraethylphenosafranine and 200 ml deionized water. The mixture was stirred for several minutes to dissolve the dye as completely as possible. Methylene chloride (40 ml) was then added, and the system was flushed with argon. The pH was adjusted to 10 with 20% aqueous NaOH, and 8.0 g (0.046 M) sodium dithionite was added all at once as a solid. The pH dropped to between about 3-4 and the solution decolorized over several minutes to an olive-green color. The solution was stirred for about 20 minutes. The acid chloride, 9.69 g (0.035 M) p-(phenylsulfonyl)benzoylchloride, ground to a fine powder and suspended in 60 ml methylene chloride, was added dropwise over a period of 30-45 minutes, the pH being adjusted continuously with NaOH solution to keep it between 3 and 4.5.
After the addition of acid chloride, about 25 ml methylene chloride was used to rinse the residual acid chloride into the flask. The mixture was stirred for about 3 hours. The pH was then adjusted to between 9.5 and 10 and the solution was stirred an additional hour. The methylene chloride layer was isolated from the water layer (pH 10) and washed once with 5% NaOH solution. The solution was dried over CaSO.sub.4 and the methylene chloride was stripped leaving about 10.36 g (69%) crude product. Decolorizing three times with Attapulgus clay yielded a light yellow-brown methylene chloride solution which, upon removal of solvent, gave about 5.2 g product (35%).
Example Ii
This example demonstrates the preparation of N-[8-[bis(2-cyanoethyl)amino]-5-[4-(phenylsulfonyl)-benzoyl]-5,10-dihydro- 10-phenyl-2-phenazinyl]-4-phenylsulfonyl)benzamide (leuco dye no. 13 of Table I) and the preparation of its dye precursor.
A 3-liter round-bottomed flask fitted with a mechanical stirrer was loaded with 16.6 g (0.066 mole) of 4-(bis-2(cyanoethyl)amino) aniline in 800 ml of distilled water. A 10% excess of aniline (13.56 g, 0.1456 mole) and 200 ml of distilled water were added to the mixture. the mixture was cooled to 0.degree. C. in an ice bath, and 10 g concentrated hydrochloric acid in 25 ml of water were added. Then 6.31 g (0.0883 mole) of sodium dichromate in 25 ml of water was added. The temperature rose to 7.degree. C. Stirring was continued as 9 ml of concentrated hydrochloric acid in 25 ml of distilled water was added over a period of two hours. After 16 hours the temperature had risen to 20.degree. C. The mixture was heated under reflux for 4 hours and then filtered hot. The filter cake was washed with 1.5 liters of boiling water. The combined filtrates were concentrated to 1.4 liters by vacuum evaporation, and then heated to 75.degree. C. as 200 g of sodium chloride were added.
The mixture was cooled to room temperature, chilled in an ice bath, and the solid was then recovered by filtration to give 14.6 g (yield=51.6%). (.lambda.max-537 nm in methanol).
A 1 liter 3 necked flask was fitted with a Claisen head with two dropping funnels, a mechanical stirrer, and a pH electrode. A solution containing 5.0 g (0.012 mole) of the dye prepared above, 210 ml of water and 0.2 g of ethylene diamine tetraacetic acid was added to the flask and stirred, while 250 ml of methylene chloride was added. The system was closed and flushed with argon, the pH adjusted to 10, then 2.44 g (0.014 mole) of sodium dithionite was added. The solution turned orange and the pH dropped to 3.7. Aqueous sodium hydroxide solution (25%) was added to bring the pH to 4.5, and then 7.53 g (0.027 mole) of 4-phenyl sulfonyl benzoyl chloride in 60 ml of methylene chloride was added dropwise. The pH was maintained between 4 and 5. After 11/2 hours, the pH was raised to 10-11. After an additional 50 minutes, the methylene chloride layer was removed and dried over calcium sulfate. The solution was treated with about 10 g of Attapulgus clay and filtered. The solvent was then evaporated, leaving 8.14 g of solid (79% yield).
Example Iii
This example demonstrates how thermally imageable films prepared with similar imaging compositions but containing leuco dyes differing only in the substituents at the 10-position, i.e. R.sup.1, exhibit differing stabilities on the stage of an overhead projector. The stability of the leuco forms in the imageable films on an overhead projector is directly related to the time that the unimaged areas, i.e. "background" areas, remain relatively low in density. A background density reading of greater than 0.1 on any filter is normally considered the point of failure.
Formulations A and B were prepared by mixing the following ingredients in the amounts indicated:
Formulation A was coated at 3 mil (75 .mu.m) wet thickness on a 4 mil (100 .mu.m) polyester film and dried for 3 minutes at 140.degree. F. (60.degree. C.). Formulation B was coated at 3 mil (75 .mu.m) wet thickness on a 4 mil (100 .mu.m) polyester film and dried for 4 minutes at 130.degree. F. (54.degree. C).
Test images were formed by means of infrared imaging in a 3M Model 45 Infrared Transparency Maker.
A 3M Model 66 overhead projector was used in conducting the image stability tests. The Model 66 had a high wattage bulb (615 watts) and gave a relatively high stage temperature (65.degree. C.).
Background image densities were measured with a MacBeth Densitometer Model TD504. Maximum image dye densities of about 1.0 were used in all cases. Background image densities after various periods of time on the stage of the Model 66 overhead projector are recorded in Table II:
The p-(phenylsulfonyl)-benzoyl group of leuco dye no. 9 is more electron-withdrawing than the 3,4-dichlorobenzoyl group of leuco dye no. 2 and the stage life of dye no. 9 is much greater than the stage life of leuco dye no. 2.
Comparative Example A
This Example demonstrates the relative instability of the unsubstituted benzo form of the same dye used in Example III i.e. R.sup.1 = ##STR52## with R.sup.2, R.sup.3, R.sup.4, R.sup.5, R.sup.6, R.sup.7, R.sup.8, R.sup.9, R.sub.10, R.sup.11, R.sup.12, being identical to those in leuco dyes no. 9 (Table I) and no. 2 (Table I) the stabilities of which were demonstrated in Example III. Formulation C was prepared by mixing the following ingredients in the amounts indicated:
Formulation C was coated at 3 mil (75 .mu.m) wet thickness on a 4 mil (100 .mu.m) polyester film and dried for 5 minutes at 120.degree. F. (49.degree. C.). This coating was then overcoated with the following composition:
The overcoat composition was coated at 3 mil (75 .mu.m) wet thickness and dried for 5 minutes at 120.degree. F. (49.degree. C. usable film could be prepared only by coating the nitrate oxidant and the leuco dye in separate layers.
Background image densities after various periods of time on the stage of the Model 66 overhead projector are recorded in Table III.
Because a background density in excess of 0.10 on any filter is normally considered to indicate the point of failure, from the foregoing Table, it can be seen that stage life is less than one hour. The dye in this comparative example is less stable than the dyes in Example III.
Example Iv
Leuco dyes no. 11 (Table I) and no. 13 (Table I) were prepared from the same starting dye form, as was the unsubstituted benzoyl leuco form, i.e., where R.sup.1 and R.sup.5 are ##STR53## and R.sup.2, R.sup.3, R.sup.4 and R.sup.6 are identical to those substituents in leuco dyes no. 11 and no. 13. The starting dye form is shown below: ##STR54##
The unsubstituted benzoyl leuco dye could be coated without backgrounding only by adding diphenylamine to the formulation. The coating formulations for the unsubstituted benzoyl leuco dye and for leuco dyes no. 11 and no. 13 are set forth below:
Formulations D and F were coated onto 4 mil (100 .mu.m) polyester film at 3 mil (75 .mu.m) wet thickness and dried at 120.degree. F. (49.degree. C.). for 5 minutes. Formulation E was coated onto 4 mil (100 .mu.m) polyester film at 3 mil (75 .mu.m) wet thickness and dried at 132.degree. F. (56.degree. C.) for 4 minutes.
Background image densities after various periods of time on the stage of the Model 66 overhead projector are recorded in Table IV:
Even with the additional stabilizer present, the stage life of Formulation D was less than 1 hour. The 3,4-dichlorobenzoyl leuco dye of Formulation E was of intermediate stability, showing backgrounding after 6 hours. The p-phenylsulfonyl benzoyl leuco dye of Formulation F showed the greatest stability. Although the image density on the blue filter had a high initial value, it changed only slightly after 16 hours on the stage.
Example V
This example demonstrates that in leuco dyes of the present invention having acyl groups at positions R.sup.5 and R.sup.1 (of Formula I), the electron-withdrawing substituent at position 10, i.e., R.sup.1, is most responsible for the enhanced stability of the leuco dye. In the formulations described below, a small amount of yellow leuco dye 2,3-dihydro-1,3,3-trimethyl-2-[2-(2,4,6-trimethoxyphenyl) ethenyl]-1H-indole, was added to each formulation to alter the image color. The coating formulations were as follows:
Formulations G and H were coated onto 4 mil (100 .mu.m) polyester film at 3 mil (75 .mu.m) wet thickness and dried at 165.degree. F. (74.degree. C.) for two minutes. Background image densities as a function of time on the stage of the Model 66 overhead projector are shown in Table V.
Leuco dye no. 14 is essentially identical to leuco dye no. 13 with respect to stability, even though the benzoyl group at the 3-position (R.sup.5) does not contain an electron-withdrawing substituent.
Example Vi
This Example demonstrates that the leuco dyes of the present invention exhibit increased stability in the coating formulations themselves, in addition to exhibiting increased stability to both thermal and actinic effects when coated on a substrate. In other words, the "pot-life" of the coating formulations for leuco phenazines dyes containing strong electron-withdrawing groups at the 10-position is longer than the "pot-life" of coating formulations containing leuco phenazine dyes that have weak electron-withdrawing substituents at the 10-position. The following formulations were prepared to illustrate this feature.
The approximate pot lives of the formulations are listed in Table VI.
Various modifications and alterations of this invention will become apparent to those skilled in the art without departing from the scope and spirit of this invention and it should be understood that this invention is not to be unduly limited to the illustrative embodiments set forth herein.
Claims
What is claimed is:
1. A leuco phenazine dye having the structural formula: ##STR55## wherein R.sup.1 represents a member selected from the group consisting of: I. aryl groups having up to 10 carbon atoms and containing from 1 to 5 electron withdrawing substituents, wherein said electron withdrawing substituents are selected from the group consisting of either: A. sustituents which are overall electron withdrawing independent of their position on the aryl radical, said electron withdrawing substituents being selected from the group consisting of: 1. --SO.sub.2 R.sub.17 2. trifluoroalkyl groups having up to 10 carbon atoms II. alkyl groups selected from the group consisting of --CH.sub.2 Cl and --CHCl.sub.2, R.sub.2 represents a member selected from unsubstituted alkyl and aryl groups having up to 10 carbon atoms and substituted alkyl and aryl groups having up to 10 carbon atoms, wherein said substituents on said alkyl groups can be methoxy groups and said substituents on said aryl groups can be selected from the group consisting of methoxy and methyl, R.sub.3, R.sub.4, R.sub.5 and R.sub.6 independently represent members selected from the group consisting of: ##STR56## and substituted and unsubstituted alkyl groups having 1 to 6 carbon atoms wherein said substituents are selected from the group consisting of halogens, --CN, hydroxy, and alkoxy having 1 to 10 carbon atoms, R.sup.7, R.sup.8, R.sup.9, R.sup.10, R.sub.11 and R.sup.12 independently represent members selected from the group consisting of hydrogen, halogen, unsubstituted alkyl groups, unsubstituted alkoxy groups having up to 4 carbon atoms, substituted alkyl groups having up to 4 carbon atoms, and substituted alkoxy groups having up to 4 carbon atoms, wherein said substitutents are selected from halogen, and R.sup.17 represents a member selected from the group consisting of unsubstituted alkyl and aryl groups having up to 10 carbon atoms.
2. The leuco phenazine dye of claim 1 wherein said electron withdrawing substituent is:
3. The leuco phenazine dye of claim 1 wherein said electron withdrawing groups are fluorinated alkyl groups having up to 10 carbon atoms.
4. The leuco phenazine dye of claim 1 wherein R.sup.1 represents ##STR57## R.sup.2 represents ##STR58## R.sup.3, R.sup.4, R.sup.5, R.sup.6 represents unsubstituted alkyl groups having 1 to 4 carbon atoms, and R.sup.7, R.sup.8, R.sup.9, R.sup.10, R.sup.11, and R.sup.12 represent hydrogen.
5. The leuco phenazine dye of claim 1 wherein R.sup.1 represents ##STR59## R.sup.2 represents ##STR60## R.sup.3, R.sup.4, R.sup.5, R.sup.6 represent alkyl groups having 1 to 4 carbon atoms, and R.sup.7, R.sup.8, R.sup.9, R.sup.10, R.sup.11, and R.sup.12 represent hydrogen.
Patent Citations (14)
| Patent | Date | Inventor | Cited By |
|---|---|---|---|
| US2783227 | 1957-02-01 | Adams et al. | |
| US2783228 | 1957-02-01 | Adams et al. | |
| US3873340 | 1975-09-01 | Miyazawa et al. | |
| US4309255 | 1982-01-01 | Gentler et al. | |
| US4379835 | 1983-04-01 | Lowrey et al. | |
| US4386154 | 1983-05-01 | Smith et al. | |
| US4423139 | 1983-12-01 | Isbrandt et al. | |
| US4460677 | 1984-07-01 | Smith et al. | |
| EPX181085 | |||
| DEX2154659 | 1972-05-01 | ||
| DEX2154660 | 1972-05-01 | ||
| JPX52-25330 | 1977-07-01 | ||
| WOX81-01757 | 1981-06-01 | ||
| GBX1271289 | 1972-04-01 |
Non-Patent Literature (2)
- Miller et al, Chem. Abs. 105, 105822j (5-14-86).
- Search Report for European Patent Application 85306998.7.