WO1989010384A1 - Lightfast disperse dyestuffs - Google Patents

Lightfast disperse dyestuffs Download PDF

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Publication number
WO1989010384A1
WO1989010384A1 PCT/US1989/001693 US8901693W WO8910384A1 WO 1989010384 A1 WO1989010384 A1 WO 1989010384A1 US 8901693 W US8901693 W US 8901693W WO 8910384 A1 WO8910384 A1 WO 8910384A1
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Prior art keywords
disperse
photostabilizer
hybrid
dyestuff
structural unit
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PCT/US1989/001693
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French (fr)
Inventor
Harold Stanley Freeman
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North Carolina State University
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    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
    • C09B29/00—Monoazo dyes prepared by diazotising and coupling
    • C09B29/0003—Monoazo dyes prepared by diazotising and coupling from diazotized anilines
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
    • C09B1/00—Dyes with anthracene nucleus not condensed with any other ring
    • C09B1/50—Amino-hydroxy-anthraquinones; Ethers and esters thereof
    • C09B1/51—N-substituted amino-hydroxy anthraquinone
    • C09B1/514—N-aryl derivatives
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
    • C09B1/00—Dyes with anthracene nucleus not condensed with any other ring
    • C09B1/50—Amino-hydroxy-anthraquinones; Ethers and esters thereof
    • C09B1/51—N-substituted amino-hydroxy anthraquinone
    • C09B1/515—N-alkyl, N-aralkyl or N-cycloalkyl derivatives
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
    • C09B29/00—Monoazo dyes prepared by diazotising and coupling
    • C09B29/06—Monoazo dyes prepared by diazotising and coupling from coupling components containing amino as the only directing group
    • C09B29/08—Amino benzenes
    • C09B29/0805—Amino benzenes free of acid groups
    • C09B29/0807—Amino benzenes free of acid groups characterised by the amino group
    • C09B29/0809—Amino benzenes free of acid groups characterised by the amino group substituted amino group
    • C09B29/0811—Amino benzenes free of acid groups characterised by the amino group substituted amino group further substituted alkylamino, alkenylamino, alkynylamino, cycloalkylamino aralkylamino or arylamino
    • C09B29/0813—Amino benzenes free of acid groups characterised by the amino group substituted amino group further substituted alkylamino, alkenylamino, alkynylamino, cycloalkylamino aralkylamino or arylamino substituted by OH, O-C(=X)-R, O-C(=X)-X-R, O-R (X being O,S,NR; R being hydrocarbonyl)
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
    • C09B51/00—Nitro or nitroso dyes
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
    • C09B69/00—Dyes not provided for by a single group of this subclass

Abstract

A method of producing a UV lightfast disperse dyestuff comprising selecting a disperse dyestuff having predetermined chromophoric groups, selecting a photostabilizer compound, designing a hybrid disperse dye molecular structure which contains the chromophoric groups of the selected disperse dyestuff and also contains the molecular structural features of the selected photostabilizer compound, and synthesizing the thus designed hybrid disperse dyestuff molecule. Such a method produces a hybrid dye molecule which is a UV lightfast analog of a disperse dyestuff having predetermined chromophoric groups, said hybrid dye molecule containing in its molecular structure the chromophoric groups of the selected disperse dyestuff and also containing the molecular structural features of a photostabilizer compound.

Description

LIGHTFAST DISPERSE DYESTUFFS Field and Background of the Invention This invention relates to lightfast disperse dyestuffs and to methods of designing and preparing such dyestuffs. In particular, this invention relates to disperse dyestuffs which are so designed that their molecular structures impart lightfastness to the dyestuff.
Disperse dyestuffs were developed for use in dyeing hydrophobic synthetic fibers such as cellulose acetate, nylon, polyester and acrylics. In recent years considerable development has been directed to producing new disperse dyestuffs with improved properties for many new applications.
One of the most important considerations in determining the suitability of dyestuffs for specific applications is lightfastness. Dyes tend to undergo photodegradation upon exposure to light, especially light in the ultraviolet spectrum, resulting in fading of the dyed textile fibers. Automobile upholstery fabrics, for example, are used in perhaps one of the most severe and demanding environments for dyestuffs. Automobile interiors may be exposed to direct sunlight over extended periods of time, and may encounter extreme high temperatures and humidities. Consequently, automobile upholstery fabrics require optimum lightfastness. Most of the disperse dyestuffs presently available do not provide the high level of lightfastness demanded in automotive applications, especially where relatively dark colors are required.
Efforts to improve the lightfastness of disperse dyed fibers have been directed primarily to the use of photostabilizer additives, such as UV absorber compounds. The most commonly used photostabilizers include benzophenones, benzotriazoles, and hindered amines. These compounds are typically applied to the fiber during the dyeing process by mixing the photostabilizer compound in the dyebath with the dyestuffs and with other conventional dyebath additives. The photostabilizer compound is adsorbed into the fibers along with the dyestuff molecules and serves to protect the dyestuff molecules from the destructive effects of the energy from absorbed UV light. The mechanisms involved in the photostabilization of a disperse dyestuff molecule by photostabilizer compounds have been extensively studied and reported in the literature and will not be treated here. Suffice it to say that in the photostabilization mechanism, it is important that the photostabilizer compound be in close proximity to the chromophoric group of the dyestuff in order that it can serve to protect the dyestuff molecule from photodegradation.
Summary of the Invention The present invention is a departure from the conventional approaches to improving lightfastness through the use of photostabilizer additives in the dyebath. The present invention, moreover, provides an approach to the design of disperse dyestuffs based upon incorporating the structural features of effective photostabilizers into the molecular structure of the dyestuff molecule itself. The ' dyestuff molecules possess the desirable lightfastness properties of a photostabilizer while maintaining the necessary chromophoric and substantive properties of a disperse dyestuff. In this sense, disperse dyestuffs according to the present invention may be viewed as "hybrid" dyestuffs which have been specifically designed and engineered to function both as a photostabilizer and as a dyestuff. Each individual dyestuff molecule is assured of having its chromophoric groups in close proximity to a photostabilizer, since the hybrid dyestuff molecule has built into it the molecular structural features of an effective photostabilizer.
In accordance with the present invention, lightfast disperse dyestuffs are produced by first selecting a "model" or "prototype" disperse dyestuff having predetermined chromophoric groups, and also selecting a photostabilizer compound having photostabilization properties. A hybrid disperse dyestuff molecular structure is designed which contains the chromophoric groups of the selected disperse dyestuff and also contains the molecular structural features of the selected photostabilizer compound, and the thus designed hybrid disperse dyestuff molecule is synthesized.
Detailed Description of the Invention The photostabilizers which are most preferred for incorporation into the dyestuffs of the present invention are those photostabilizer compounds which have heretofore been used as photostabilizer additives to dyebaths in conventional dyeing processes. These photostabilizer compounds generally fall into one of three main structural types: the benzophenones, having the general structural formula:
Figure imgf000006_0001
where R = H, OH, OMe and CH3 and 2 = H, OH, OMe and CH3 ■ the benzotriazoles, having the general structural formula:
Figure imgf000007_0001
where Rx = H, OH, OMe, NH2, CH3, and Cl and R2 = H, NH2, CH3, and C(CH3)3 and the hindered amines, whose general structural formula is as follows:
Figure imgf000007_0002
5 where R = H, OH, NH2 and amino alkyl
Disperse dyestuffs may be classified chemically as aminoazobenzenes (azo dyes) , aminoanthraquinones (anthraquinone dyes) and nitrodiarylamines (nitro dyes) . The characteristic structural unit of azo
■jQ dyes is the -N=N- chromophoric group, and this classification of dyes includes monoazo, disazo, trisazo and tetrakisazo dyes, according to the number of -N=N- groups present in the dye molecule. The characteristic structural unit of the
*I5 anthraquinone dyes is anthraquinone:
Figure imgf000008_0001
including the chromophoric groups: _____ C=0 and -C=C**^ • The nitro dyestuffs are characterized by the structural unit ArN02.
In designing the molecular structure of dyestuffs in accordance with the present invention, it is desirable to keep the molecular structures as compact and small as possible in order to get optimum penetration and adsorption into the fibers. Therefore, hybrid molecular structures in which the photostabilizer moiety is incorporated into the dyestuff structure are preferred over structures which would result from attachment of a ~ photostabilizer molecule to a dyestuff molecule through a bridging group. For example, upon examining the molecular structural features of Disperse Yellow 42
Figure imgf000008_0002
and a typical benzophenone:
Figure imgf000009_0001
it will be seen that through the addition of a hydroxybenzoyl group to the dyestuff molecule, a benzophenone moiety can be generated in the structure, yielding lightfast analogs of Disperse Yellow 42 such as the following:
Figure imgf000009_0002
Figure imgf000009_0003
In this instance, one of the phenyl groups present in the dyestuff molecule is shared by the benzophenone moiety. Thus, this approach to designing a lightfast disperse dyestuff entails examining the molecular structure of the selected dyestuff and the selected photostabilizer compound to identify an atom or group of atoms common to both and designing a hybrid disperse dyestuff molecular structure which includes the structural features of both the selected dyestuff and the selected photostabilizer and which shares the identified common atom or group of atoms. The thus designed hybrid disperse dyestuff is then synthesized by
10 selecting appropriate intermediates and reacting them to produce the desired molecular structure.
Light stabilized dyestuffs can also be produced by incorporating a benzotriazole structure into the molecular structure of a dyestuff such as Red Dye
15 167 as illustrated by the following azo dyestuff structures:
Figure imgf000010_0001
Disperse Red 167 Benzotriazole analog of Disperse Red 167
In this instance, the -N(CH2CH20Ac)2 group of the
20 prototype dyestuff is replaced by the benzotriazole moiety and the pendant nitrogen atom is shared by the molecular structures of the dyestuff portion and the photostabilizer portion.
Light stabilized dyestuffs can also be produced by incorporating a hindered amine moiety into the molecular structure of a dyestuff as illustrated by the following anthraquinone dyestuff structures:
Figure imgf000011_0001
Disperse Blue 27 Hindered amine analog of Disperse Blue 27 In this instance, the -hydroxyethylphenyl group of the prototype dyestuff is replaced by the hindered amine moiety, which is somewhat similar in structure, but possesses photostabilizer properties.
The full scope of the present invention, and the broad range of dyestuffs which can be produced thereby, will be understood more fully from the illustrative examples which follow:
Hybrid Nitro Dyestuffs With Benzophenone Photostabilizers
Example 1
The nitro dyestuff Disperse Yellow 42
Figure imgf000012_0001
was selected as the prototype dyestuff for which a UV lightfast analog would be prepared. The photostabilizer 2-hydroxy-4-methoxybenzophenone
Figure imgf000012_0002
was selected as the benzophenone photostabilizer. The molecular structures of these compounds were examined to identify an atom or group of atoms that would be made common to the dyestuff and the photostabilizer, and the unsubstituted phenyl group was identified. Thus a hybrid disperse dyestuff molecule was designed" as follows:
Figure imgf000012_0003
where the bracketed phenyl group is shared as the common group. This hybrid disperse dyestuff molecule, which is an analog of Disperse Yellow 42, contains molecular structural features of the dyestuff including the chromophoric group -N02 and molecular structural features of the benzophenone photostabilizer compound. Example 2
The prototype nitro dyestuff was Disperse
Yellow 42 as in Example 1 and 2-hydroxy-4- methoxybenzophenone
Figure imgf000013_0001
was selected as the photostabilizer. After examining both molecular structures, it can be seen that by adding the appropriate hydroxymethoxybenzoyl group to the dyestuff, the benzophenone moiety can be generated in the dyestuff structure. Thus the 'following hybrid disperse dyestuff molecule was designed:
Figure imgf000013_0002
It will be seen that a benzophenone photostabilizer structure can also be provided at both sides of the dyestuff structure. Thus, another hybrid disperse dyestuff molecule was designed as follows:
Figure imgf000013_0003
By utilizing a nitro dye like Disperse Yellow 42 and a benzophenone photostabilizer having the general structure:
Figure imgf000014_0001
where R and R2 are H, OH and OMe, and a number of other hybrid disperse dyestuff molecules can be designed. Exemplary general structures include:
Figure imgf000014_0002
where Rx = H, OH and OMe and R2 = H, OH and OMe
Hybrid Nitro Dyestuffs With A - Benzotriazole Photostabilizer
Example 3
The prototype nitro dyestuff was Disperse
Yellow 42 and the following benzotriazole photostabilizer was selected:
Figure imgf000015_0001
The identified common group of atoms in both the dyestuff and the photostabilizer is a phenyl group. The following hybrid disperse dyestuff was designed:
Figure imgf000015_0002
Other hybrid dyestuff molecules with benzotriazole photostabilizers can be synthesized by using different benzotriazole compounds having the general formula:
Figure imgf000015_0003
where x = H, OH, OMe, NH2, CH3, and Cl and R2 = H, NH2, CH3; and C(CH3)3 Hybrid Nitro Dyestuffs With A Hindered Amine Photostabilizer
Example 4
The prototype nitro dyestuff was Disperse Yellow 42 and the following hindered amine photostabilizer, amine 4-amino-2, 2, 6, 6- tetramethylpiperidine
Figure imgf000016_0001
was selected as the photostabilizer. The following hybrid dyestuff molecule was designed:
Figure imgf000016_0002
This dyestuff molecule contains the molecular structural features of the hindered amine photostabilizer and the molecular structural features of the Disperse Yellow 42 nitro dyestuff, including the -N02 chromophoric group thereof. Hybrid Azo Dyestuffs With Benzophenone Photostabilizers
Example 5
The azo dyestuff Disperse Red 167
Figure imgf000017_0001
was selected as the prototype dyestuff. The benzophenone stabilizer 2-hydroxy-4- methoxybenzophenone
Figure imgf000017_0002
was selected as the photostabilizer. A hybrid disperse dyestuff molecule of the following structure was designed:
Figure imgf000017_0003
Although this dyestuff contains a benzoyi group in place of the acetamide group of Disperse Red 167, the same type interaction between the azo linkage and the benzoyl group that occurs between the azo linkage and the acetamide group will occur upon exposure to light.
The designed hybrid dyestuff contains the molecular structural features of the benzophenone photostabilizer and molecular structure features of the Red Dye 167 azo dyestuff, including the -N=N- chromophoric group thereof.
Example 6 The prototype azo dyestuff was Disperse Red 167 and the benzophenone photostabilizer derivative, 3- amino-2'-hydroxy- •-methoxybenzophenone
Figure imgf000018_0001
was selected. The following hybrid disperse dyestuff was designed so as to contain the molecular structural features of the Red Dye 167 and including the -N=N- chromophoric group and the molecular structural features of the benzophenone photostabilizer:
Figure imgf000018_0002
Example 7 The prototype azo dyestuff was Red Dye 167 and the benzophenone photostabilizer selected was:
Figure imgf000019_0001
A hybrid disperse dyestuff molecule of the following structure was designed:
02N (CH2CH20Ac)2
Figure imgf000019_0002
The hybrid dyestuff structure contains the molecular structural features of the benzophenone photostabilizer and the molecular structural features of Red Dye 167 azo dyestuff including the
-N=N- chromophoric group.
Hybrid Anthraquinone Dyestuffs With A Hindered Amine Photostabilizer
Example 8
The anthraquinone dyestuff Disperse Blue 27
Figure imgf000019_0003
was selected as the prototype dye. The hindered amine photostabilizer, amine 4-amino-2, 2, 6, 6- tetramethylpiperidine,
Figure imgf000020_0001
A hybrid dyestuff molecule having the following structure was designed:
Figure imgf000020_0002
This dyestuff molecule has the molecular structural features of the hindered amine photostabilizer and the molecular structural features of Disperse Blue 27, including the chromophoric groups thereof. Example 9
A blue anthraquinone dyestuff, Disperse Blue 56
Figure imgf000021_0001
was selected as the prototype dyestuff. The benzophenone photostabilizer derivative, 3-amino-2'- hydroxy-4 '-methoxybenzophenone
Figure imgf000021_0002
was selected. The hybrid disperse dyestuff molecule designed was:
Figure imgf000021_0003
This dyestuff molecule has the molecular structural features of the benzophenone photostabilizer and the molecular structural features of the anthraquinone dye, Disperse Blue 56, including the chromophoric groups thereof.
Hybrid Anthraquinone Dyestuff With A Benzophenone Photostabilizer
Example 10 A blue anthraquinone disperse dyestuff, Disperse Blue 27
Figure imgf000022_0001
was selected as the prototype dyestuff. The benzophenone photostabilizer derivative selected was 3-amino-2*-hydroxy-4*-methoxybenzophenone:
Figure imgf000022_0002
A hybrid disperse dyestuff molecule of the following structure was designed:
Figure imgf000022_0003
This dyestuff contains the molecular structural features of the benzophenone photostabilizer and the molecular structural features of the anthraquinone dyestuff, Disperse Blue 27, including the chromophoric groups thereof.
Synthesis of Hybrid Nitro Dyestuffs Example 11 The synthesis of the hybrid disperse dyestuff designed in Example 1 required the dyestuff intermediate
Figure imgf000023_0001
The required aminomethoxyhydroxybenzophenone photostabilizer intermediate was prepared by the reaction:
Figure imgf000023_0002
Pd/c
Figure imgf000023_0003
The dyestuff intermediate and the photostabilizer were combined in the reaction:
Figure imgf000024_0001
Figure imgf000024_0002
Example 12 The hybrid disperse dyestuff designed-in Example 4 was synthesized by the reaction of a nitrodiphenylamine sulfonyl chloride and a hindered amine photostabilizer, amine 4-amino-2, 2, 6, 6- tetramethylpiperidine :
Figure imgf000024_0003
Figure imgf000024_0004
Figure imgf000024_0005
Synthesis of Hybrid Azo Dyestuffs
Example 13
The hybrid disperse dyestuff designed in
Example 5 was synthesized by starting with 3-nitro-
2*-hydroxy-4'-methoxybenzophenone
Figure imgf000025_0001
and used in the reaction:
Figure imgf000025_0002
Na2S
Figure imgf000025_0003
Figure imgf000025_0004
Figure imgf000025_0005
(ρH 5) Example 14 The hybrid disperse dyestuff designed in Example 6 was synthesized by the reaction of an azo dyestuff intermediate:
Figure imgf000026_0001
and the diazσnium salt of the benzophenone photostabilizer derivative 2-amino-4- nitrobenzophenone.
Example 15 - The hybrid disperse dyestuff designed in Example 7 was synthesized by first preparing the selected benzophenone photostabilizer derivative:
Figure imgf000026_0002
This compound was diazotized using HN02 and added to the azo dyestuff intermediate of Example 14 at a pH of 5 to form the hybrid dyestuff:
(CH2CH2OAc)2
Figure imgf000027_0001
Synthesis of Hybrid Anthraquinone Dyestuffs Example 16
*» The hybrid disperse dyestuff designed in
Example 9 was prepared by reacting 4,8- dinitroanthrarufin with 3-amino-2 '-hydroxy-4 ■- methoxybenzophenone in the presence of heat followed by reduction with Na2S.
Example 17
The hybrid disperse dyestuff designed in
Example 10 was prepared by reacting 4,5- dinitrochrysazine with 3-amino-2 *-hydroxy-4 '-methoxybenzophenone in the presence of heat.
Example 18
A fabric sample dyed with the hybrid disperse dyestuff designed in Example 1 and synthesized in Example 13
Figure imgf000027_0002
was exposed to 233.2 kilojoules per square meter of UV light. A fabric sample dyed with Disperse Yellow 42 was also exposed to the same amount of UV light. Using a lightfastness rating based on a scale of 1 to 5 with a desired lightfastness rating of 5 indicating no change, the samples were compared. The hybrid dyestuff had a lightfastness rating of 3.3 and the Disperse Yellow 42 dyestuff had a lightfastness rating of 1.5. As is readily apparent from the foregoing examples, a multiplicity of hybrid dyestuffs can be designed and synthesized by practice of the present invention. These examples are provided as illustrations of the broad scope of the principles, preferred embodiments and modes of operation of the present invention. The invention which is intended to be protected herein, however, should not be construed as limited to the particular forms disclosed since those are to be regarded as illustrative rather than restrictive. Variations and changes may be made by those skilled in the art without departing from the spirit of the invention, particularly with respect to the choice of other specific azo, anthraquinone and nitro dyes and other specific photostabilizer compounds.

Claims

THAT WHICH IS CLAIMED IS:
1. A method of producing a UV lightfast disperse dyestuff comprising selecting a disperse dyestuff having predetermined chromophoric groups, selecting a photostabilizer compound, designing a hybrid disperse dye molecular structure which contains the chromophoric groups of the selected disperse dyestuff and also contains the molecular structural features of the selected photostabilizer compound, and synthesizing the thus designed hybrid disperse dyestuff molecule.
2. A method according to Claim 1 wherein the step of selecting a photostabilizer compound comprises selecting a photostabilizer compound from the class consisting of benzophenones, benzotriazoles and hindered amines.
3. A method according to Claim 1 wherein the step of selecting a disperse dyestuff comprises selecting a disperse dyestuff from the class consisting of azo dyes, anthraquinone dyes and nitro dyes.
4. A method according to Claim 1 wherein the disperse dyestuff is selected from the class consisting of azo dyes and nitro dyes and the photostabilizer compound is selected from the group consisting of benzophenones and benzotriazoles.
5. A method according to Claim 1 wherein the hybrid disperse dye molecular structure includes an anthraquinone dye structural unit and a benzophenone photostabilizer structural unit.
6. A method according to Claim 1 wherein the hybrid disperse dye molecular structure includes an anthraquinone dye structural unit and a hindered amine photostabilizer structural unit.
7. A method according to Claim 1 wherein the hybrid disperse dye molecular structure includes an azo dye structural unit and a benzotriazole photostabilizer structural unit.
8. A method according to Claim 1 wherein the hybrid disperse dye molecular structure includes an azo dye structural unit and a benzophenone photostabilizer structural unit.
9. A method according to Claim 1 wherein the hybrid disperse dye molecular structure includes a nitro dye structural unit and a benzotriazole photostabilizer structural unit.
10. A method according to Claim 1 wherein the hybrid disperse dye molecular structure includes a nitro dye structural unit and a benzophenone photostabilizer structural unit.
11. A method according to Claim 1 wherein the hybrid disperse dye molecular structure includes a nitro dye structural unit and a hindered amine photostabilizer structural unit.
12. A method of producing a disperse dye having UV lightfast properties comprising selecting a disperse dyestuff from the class consisting of azo dyes, anthraquinone dyes and nitro dyes, selecting a photostabilizer compound from the class consisting of benzophenones, benzotriazoles and hindered amines, designing a hybrid disperse dye molecular structure which includes the structural features of both the selected dyestuff and the selected photostabilizer compound, and synthesizing the thus designed hybrid disperse dyestuff molecule.
13. A method of producing a disperse dye having UV lightfast properties comprising selecting a disperse dyestuff from the class consisting of azo dyes, anthraquinone dyes and nitro dyes, selecting a photostabilizer compound, examining the molecular structure of each to identify an atom or group of atoms common to both, designing a hybrid disperse dye molecular structure which includes the structural features of both the selected dyestuff and the selected photostabilizer and which shares the identified common atom or group of atoms, and synthesizing the thus designed hybrid disperse dyestuff molecule.
14. A method according to Claim 13 wherein the atom or group of atoms common to the dyestuff and the photostabilizer comprises a phenyl group, and the selected photostabilizer comprises a benzophenone.
15. A method according to Claim 13 wherein the atom or group of atoms common to the dyestuff and the photostabilizer comprises an aniline group, and the selected photostabilizer comprises a benzophenone.
16. A method according to Claim 13 wherein the atom or group of atoms common to the dyestuff and the photostabilizer comprises a -NH group, and the selected photostabilizer comprises a benzophenone.
17. A method of producing a disperse dye having UV lightfast properties comprising selecting an azo or nitro disperse dyestuff, selecting a benzophenone photostabilizer compound, examining the molecular structure of each to identify a phenyl group ring common to the molecular structure of both the selected dyestuff and the selected benzophenone, designing a hybrid disperse dye molecular structure which includes the structural features of both the selected dyestuff and the selected benzophenone photostabilizer and which shares the identified common phenyl group, and synthesizing the thus designed hybrid disperse dyestuff molecule.
18. A hybrid disperse dye molecule which is a UV lightfast analog of a disperse dyestuff having predetermined chromophoric groups, said hybrid dye molecule containing in its molecular structure the chromophoric groups of the selected disperse dyestuff and also containing the molecular structural features of a photostabilizer compound.
19. A hybrid disperse dye molecule according to Claim 18 in which the photostabilizer compound is selected from the class consisting of benzophenones, benzotriazoles and hindered amines.
20. A hybrid disperse dye molecule according to Claim 18 in which the disperse dyestuff is selected from the class consisting of azo dyes, anthraquinone dyes and nitro dyes.
21. A hybrid disperse dye molecule according to Claim 18 in which the disperse dye is selected from the class consisting of azo dyes and nitro dyes and the photostabilizer compound is selected from the class consisting of benzophenones and benzotriazoles.
22. A hybrid disperse dye molecule according to Claim 18 which includes an anthraquinone dye structural unit and a benzophenone photostabilizer structural unit.
23. A hybrid disperse dye molecule according to Claim 18 which includes an anthraquinone dye structural unit and a hindered amine photostabilizer structural unit.
24. A hybrid disperse dye molecule according to Claim 18 which includes an azo dye structural unit and a benzotriazole photostabilizer structural unit.
25. A hybrid disperse dye molecule according to Claim 18 which includes azo dye structural unit and a benzophenone photostabilizer structural unit.
26. A hybrid disperse dye molecule according to Claim 18 which includes a nitro dye structural unit and a benzotriazole photostabilizer structural unit.
27. A hybrid disperse dye molecule according to Claim 18 which includes a nitro dye structural unit and a benzophenone photostabilizer structural unit.
28. A hybrid disperse dye molecule according to Claim 18 which includes a nitro dye structural unit and a hindered amine photostabilizer structural unit.
29. A textile fiber dyed with a hybrid disperse dye molecule according to Claim- 18.
30. A hybrid disperse dye molecule which is a UV lightfast analog of a disperse dye selected from the class consisting of azo dyes, anthraquinone dyes and nitro dyes, said hybrid disperse dye molecule including in its molecular structure the characteristic structural unit of the selected disperse dye and the characteristic structural unit of a photostabilizer molecule selected from the class consisting of benzophenones, benzotriazoles and hindered amines.
31. A hybrid disperse dye molecule according to Claim 30 wherein an atom or group of atoms is shared by the molecular structure of the selected disperse dye and the molecular structure of the photostabilizer.
32. A hybrid disperse dye molecule according to Claim 31 wherein the shared atom or group of atoms comprises a phenyl group.
33. A hybrid disperse dye molecule according to Claim 31 wherein the shared atom or group of atoms are located in a portion of the hybrid disperse dye molecular structure proximate to the chromophoric group of the selected disperse dye.
34. A hybrid disperse dye molecule according to Claim 30 wherein the disperse dyestuff is selected from the class consisting of azo dyes and nitro dyes and the photostabilizer compound is a benzophenone.
35. A hybrid disperse dye molecule according to Claim 30 wherein the disperse dyestuff is selected from the class consisting of azo dyes and nitro dyes and the photostabilizer compound is a benzotriazole.
36. A hybrid disperse dye molecule according to Claim 30 wherein the disperse dyestuff is selected from the class consisting of anthraquinone dyes and nitro dyes and the photostabilizer compound is a hindered amine.
37. A textile fiber dyed with a hybrid disperse dye molecule according to Claim 30.
38. A UV lightfast analog of the disperse dyestuff Disperse Yellow 42 containing in its structure a photostabilizer moiety selected from the class consisting of benzophenone, benzotriazole and hindered amines.
39. A UV lightfast analog of the disperse dyestu Disperse Red 167 containing in its structure a photostabilizer moiety selected from the class consisting of benzophenone, benzotriazole and " hindered amines.
40. A UV lightfast analog of the disperse dyestuff Disperse Blue 56 containing in its structure a photostabilizer moiety selected from the class consisting of benzophenone, benzotriazole and hindered amines.
41. A UV lightfast analog of the disperse dyestuff Disperse Blue 27 containing in its structure a photostabilizer moiety selected from the class consisting of benzophenone, benzotriazole and hindered amines.
PCT/US1989/001693 1988-04-21 1989-04-20 Lightfast disperse dyestuffs WO1989010384A1 (en)

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US184,382 1988-04-21

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WO2004101688A1 (en) 2003-05-16 2004-11-25 Canon Kabushiki Kaisha Novel coloring compound and recording material using the same
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