More specifically this invention relates to toner compositions having a polymeric polyester dye component for development of latent electrostatic charge patterns.

The formation and development of images on the surface of photoconductive materials by electrostatic means is well known. The basic electrophotographic imaging process (U.S. 2,297,691) involves placing a uniform electrostatic charge on a photoconductive insulating layer known as a photoconductor or photoreceptor, exposing the photoreceptor to a light and shadow image to dissipate the charge on the areas of the photoreceptor exposed to the light, and developing the resulting electrostatic latent image by depositing on the image a finely divided electroscopic toner material. The toner will normally be attracted to those areas of the photoreceptor which retain a charge, thereby forming a toner image corresponding to the electrostatic latent image. This developed image may then be transferred to a substrate such as paper. The transferred image subsequently may be permanently affixed to the substrate by heat, pressure, a combination of heat and pressure, or other suitable fixing means such as solvent or overcoating treatment.

Toner and developer compositions including colored developer compositions are in wide use. These compositions normally contain toner particles consisting of resin and colorants, and carrier particles. The colorants usually are selected from cyan dyes or pigments, magenta dyes or pigments, yellow dyes or pigments, and mixtures thereof.

One of the main advantages of selecting organic dyes instead of pigments for color toner compositions resides in the provisions of increased color fidelity as the dyes can be molecularly dispersed in the toner resins. To obtain a homogeneous dispersion, it is generally necessary to build into these molecules certain substituents for enhancing their compatibility with the toner resin. Unless the dye molecules are substantially fully compatible with the toner resins, they have a tendency to aggregate with time, especially when subjected to heat, pressure and humidity thereby resulting in a loss of color fidelity.

Additionally, the low molecular weight of the dye molecules causes a high lability or mobility of the dye molecules in the toner resin resulting in undesirable bleeding of the dyes.

Of particular interest with respect to the present invention are toner compositions which include a chromophoric resin ingredient. U.S. 3,699,135 describes a polymer dye prepared by the copolymerization of a silane with an anthraquinone containing two aliphatic hydroxyl groups. U.S.

4,375,357 describes water-soluble noncrystalline

polymer block colorants composed of an organic polymer backbone with pendant azo chromophoric units.

Other prior art publications which describe polymeric dyes for toner compositions include United States Patent Numbers 3,553,133; 4,645,727; 4,778,742; 5,200,290; 5,212,033; 5,296,325; and 5,437,953; incorporated by reference.

There is continuing interest in the development of new and improved toner compositions for application in electrophotography.

Accordingly, it is an object of this invention to provide a polymeric dye toner composition which has a superior combination of properties for electrophotographic imaging systems.

It is another object of this invention to provide chromophoric monomers which are adapted for preparation of polyester dyes by a copolymerization reaction.

Other objects and advantages of the present invention shall become apparent from the accompanying description and examples.

DESCRIPTION OF THE INVENTION One or more objects of the present invention are accomplished by the provision of a chromophoric monomer corresponding to the formula:

where X is -O- or -NH-; R is a covalent bond or a divalent C1-Cl6 aliphatic, alicyclic or aromatic radical; and R1 is a C1 -C6 aliphatic radical.

The R radical is illustrated by straight or branched-chain alkylene groups such as ethylene, 2- ethylhexylene, octylene and decylene; alicyclic groups such as cyclopentylene and cyclohexylene; aromatic groups such as phenylene, tolylene, xylylene, biphenylene, naphthylene, pyridylene, and the like.

The R1 radical is illustrated by substituents such as methyl, ethyl, propyl, 2-methylpropyl, hydroxyethyl, 3-hydroxy-2-methylpropyl, and the like.

A formula I chromophoric monomer can be prepared by the following type condensation reaction: O o HX---Dye--jXH + 2 Base 2 2 2 rn 2) cH30Na C1 C1 0 779 0 0 (CH2)m (CH2) CH30 XDye-X OCH3 The acyl chloride can be a difunctional reactant such as malonoyl chloride, adipoyl chloride,

sebacoyl chloride, isophthaloyl chloride, terephthaloyl chloride, and the like.

Illustrative of formula I chromophoric monomers are bis(C1-C6 alkyl sebacamide) of 6'-butoxy-2, 6-diamino-3,3'-azodipyridine; bis (methyl sebacamide) of 6' -butoxy-2,6-diamino-3,3' -azodipyridine; bis(C1-C6 alkyl sebacamide) of thionine; bis(methyl sebacamide) of thionine; bis(C1-C6 alkyl sebacamide) of basic fuchsin; bis(methyl sebacamide) of basic fuchsin; bis(C1-C6 alkyl sebacamide) of 3,6-diaminoacridine hydrochloride; bis(methyl sebacamide) of 3,6- diaminoacridine hydrochloride; bis(C1-C6 alkyl sebacate) of 4-(4-nitrophenylazo)resorcinol; bis(methyl sebacate) of 4-(4-nitrophenylazo) resorcinol; bis(C1-C6 alkyl sebacamide) of 2, 9-dimethylquinacridone; bis (methyl sebacamide) of 2,9-dimethylquinacridone; bis(C1-C6 alkyl sebacamide) of 1,4-bis(ethylamino)-9,10-anthraquinone; bis(methyl sebacamide) of 1,4-bis(ethylamino)-9,10- anthraquinone; bis(C1-C6 alkyl sebacamide) of 1,4-bis(n- butylamino)-9,10-anthraquinone; bis (methyl sebacamide) of 1,4-bis(n -butylamino-9 , lO-anthraquinone; bis(C1-C6 alkyl sebacamide) of 1,4-bis(4-methylanilino)-9,10- anthraquinone; bis(methyl sebacamide) of 1,4-bis(4- methylanilino)-9,10-anthraquinone; bis (C1-C6 alkyl sebacamide) of 2,3-dihydro-2,2-dimethyl-6- [[4- (phenylazo) -l-naphthalenyl] azo] -lH-perimidine; bis (methyl sebacamide) of 2,3-dihydro-2,2-dimethyl-6- [[4-(phenylazo)-1-naphthalenyl]azo]-lH-perimidine; and the like.

In another embodiment this invention provides a chromophoric monomer corresponding to the formula:

where X is -O- or -NH-; and R is a covalent bond or a divalent C1-Cl6 aliphatic, alicyclic or aromatic radical; and R1 is a C1-C6 aliphatic radical.

The R and R1 radicals in formula II can be similar to those illustrated for formula I monomers. A similar type of reaction can be employed for formula II monomer synthesis, such as the condensation of sebacoyl chloride and methyl eosin to produce bis(methyl eosin) sebacate.

In another embodiment this invention provides monomeric diols which can copolymerize with a formula I or formula II chromophoric monomer to form a polyester dye for toner compositions. The invention monomeric diols correspond to one of the formulas:

where R is normal or branched-chain C3-C30 alkylene; R1 is normal or branched-chain C8 -C30 alkylene; and R2 is normal C6-C28 alkyl.

Illustrative of formulas III-V monomeric diols are bis(3-hydroxy-2-methylpropyl) terephthalate; bis(2-tetradecyl-2-hydroxyethyl) terephthalate; bis (2- hexyl-2-hydroxyethyl) terephthalate; and the like.

An important aspect of the present invention is the provision of a toner composition which has a superior combination of physicochemical properties for application in electrophotographic imaging systems.

A toner composition of the present invention comprises, as a main component, a polyester dye having between about 0.1-20 mole percent of recurring chromophoric diester monomer units, and having a weight average molecular weight between about 5000-100,000, and exhibiting a glass transition temperature (Tg) between about 40"-120"C, and a melt-viscosity between about 200-5500 poises at 1500C.

In a preferred toner composition the polyester dye has a weight average molecular weight between about 10,000-30,000, and/or the toner composition has a polydispersity between about 1.2-4, and/or exhibits a melt index between about 25-1000 grams per 10 minutes at 1500C under a load of 2.16 kilograms, and/or exhibits at least 80W optical transparency at a specific wavelength within the range between about 350-750 nanometers.

The chromophoric entity in a present invention monomer or polyester dye is selected from

organic structures which include yellow 6'-butoxy-2,6- diamino-3,3'-azodipyridine; blue thionine; red basic fuchsin; magenta; 3, 6-diaminoacridine hydrochloride; red methyl eosin; yellow 4-(4-nitrophenylazo)- resorcinol; magenta 2,9-dimethylquinacridine; yellow 2,2'-[(3,3'-dichloro-l,l'-diphenyl)-4,4'-bis(azo)] bis[N-(2-methoxyphenyl)]-3-oxobutanamide; cyan 1,4- bis(ethylamino)-9,10-anthraquinone; cyan 1,4-bis(n- butylamino)-9,10-anthraquinone; cyan 1,4-bis(4- methylanilino)-9,10-anthraquinone; black 2,3-dihydro- <BR> <BR> <BR> 2,2-dimethyl-6-[[(4-phenylazo)-1-naphthylenyl]-azo]-lH- perimidine; and the like. A selected chromophoric structure has the requisite difunctionality to convert to a chromophoric monomer in accordance with the present invention.

A present invention polyester dye can be prepared by solution, suspension or non-aqueous dispersion polymerization methods. Methods for the preparation of chromophoric dyes are described in publications which include U.S. 4,645,727 and U.S. 4,778,742 and citations therein; incorporated by reference.

A present invention toner composition can include between about 0.001-2 weight percent of a charge control agent for the purpose of imparting a positive charge to toner composition particles. The toner particles typically have an average particle size between about 2-20 microns.

Suitable charge control agents include carboxylated salts such as zinc heptanoate and aluminum 2-ethylhexanoate; lecithin; polyisobutylene

succinimide; cetyl pyridinium chloride; and charge control agents disclosed in publications such as U.S.

5,200,290 and U.S. 5,296,325; incorporated by reference.

A present invention toner composition can include between about 0.1-10 weight percent of a surfactant ingredient to stabilize the toner composition particles. A preferred surfactant is a polymeric type as described in U.S. 5,200,290, such as chlorinated polypropylene and poly(ethylene-vinyl acetate).

A present invention toner composition can include between about 0.5-15 weight percent of a wax ingredient, as illustrated by beeswax, paraffin wax, montan wax, carnauba wax, microcrystalline wax, fatty alcohols, fatty esters, and the like.

A present invention toner composition also can include between about 1-30 weight percent of a particulate co-host resin such as styrene/ methacrylate copolymer, styrene/butadiene copolymer, pentaerythritol terephthalate polyester, and the like, which is interspersed with the polyester dye particles.

A present invention toner composition has superior properties for purposes of electro- photographic imaging systems. A invention toner composition is a free-flowing powder which is a stable dispersion having a long shelf and storage life.

Desirable print density and print quality, and excellent color quality, can be achieved in electrostatic image development with an invention toner composition.

The following examples are further illustrative of the present invention. The components and specific ingredients are presented as being typical, and various modifications can be derived in view of the foregoing disclosure within the scope of the invention.

EXAMPT,E I Bis(methyl sebacamide) of 6'-butoxy- 2,6-diamino-3,3'-azodipyridine (yellow) In a 500 ml three-necked flask equipped with nitrogen inlet and outlet, thermometer, condenser and mechanical stirrer, are placed 47.828 grams (0.2 m) of sebacoyl chloride and 200 grams of N-methyl-2- pyrrolidone. Sodium methoxide (10.80 grams, 0.2 m) is added into the flask. The resulting mixture is stirred at ambient temperature for 30 minutes. 6l-Butoxy-2,6- diamino-3,3'-azodipyridine (28.634 grams, 0.1 m) in 500 ml of N-methyl-2-pyrrolidone is added into the flask with fast agitation. The reaction mixture is stirred

for one hour at ambient temperature, and then poured into distilled water. The solution is basified with dilute sodium hydroxide to precipitate a yellow solid.

The recovered product is filtered, washed with water, and dried at 750 and 0.1 Torr to obtain 20.6 grams of yellow monomer with a melting point range of 1200- 1720C. The monomer is soluble in HFIP(1) AT 10%, in NMP (2) at 5%, and soluble at 5% in hot DMSO and hot ethanol.

(1) hexafluoroisopropanol.

(2) N-methyl-2-pyrrolidone.

(3) dimethylsulfoxide.

EXAMPLE IT Bis(methyl sebacamide) of thionine (blue) In a 500 ml three-necked flask equipped with nitrogen inlet and outlet, thermometer, condenser and mechanical stirrer, are placed 32.5 grams (0.1359 m) of sebacoyl chloride and 200 grams of N-methyl-2- pyrrolidone. Sodium methoxide (7.341 grams, 0.1359 m) is added into the flask. The resulting mixture is stirred at ambient temperature for 30 minutes.

Thionine (19.525 grams, 0.068 m) in 300 ml of N-methyl- 2-pyrrolidone is added into the flask with fast agitation. The reaction mixture is stirred for one hour at ambient temperature, and then poured into distilled water. The product precipitate is filtered, washed with water, and dried at 750C and 0.1 Torr to obtain 52.63 grams of viscous blue monomer. The monomer is soluble in HFIP and DMSO at 10%, in NMP at 5%, and partially soluble in ethanol.

EXAMPLE TIl <BR> <BR> <BR> Bis (methyl sebacamide) of basic fuchsin (red) In a 500 ml three-necked flask equipped with nitrogen inlet and outlet, thermometer, condenser and mechanical stirrer, are placed 47.828 grams (0.2 m) of sebacoyl chloride and 200 grams of N-methyl-2- pyrrolidone. Sodium methoxide (10.80 grams, 0.2 m) is added into the flask. The resulting mixture is stirred at ambient temperature for 30 minutes. Basic fuchsin (32.383 grams, 0.1 m) in 500 ml of N-methyl-2- pyrrolidone is added into the flask with fast agitation. The reaction mixture is stirred for one hour at ambient temperature, and then poured into distilled water. The product precipitate is filtered, washed with water, and dried at 750C and 0.1 Torr to obtain 20.6 grams of red monomer with a melting point range from 75.1° to 85.30C. The solid is soluble at 10% in HFIP, in NMP, in DMSO, and partially soluble in hot ethanol.

EXAMPLE ,F2. IV Bis(methyl sebacamide) of 3,6-dlaminoacridine hvdrochloride (magenta) In a 500 ml three-necked flask equipped with nitrogen inlet and outlet, thermometer, condenser and mechanical stirrer, are placed 47.828 grams (0.2 m) of sebacoyl chloride and 200 grams of N-methyl-2- pyrrolidone. Sodium methoxide (10.80 grams, 0.2 m) is added into the flask. The resulting mixture is stirred at ambient temperature for 30 minutes. 3,6- Diaminoacridine HCl (24.571 grams, 0.1 m) in 500 ml of N-methyl-2-pyrrolidone is added into the flask with fast agitation. The reaction mixture is stirred for one hour at ambient temperature, and then poured into distilled water. The product precipitate is filtered, washed with water, and dried at 750C and 0.1 Torr to obtain 47.87 grams of magenta monomer with a melting point range from 152.1° to 171.1°C. The solid is soluble at 10% in HFIP, partially soluble at 5% in NMP

or DMSO, and soluble in hot NMP or DMSO, and insoluble in hot ethanol.

EXAMPLE V Bis(methvl eosin) sebacate (red) In a 500 ml three-necked flask equipped with nitrogen inlet and outlet, thermometer, condenser and mechanical stirrer, are placed 4.0654 grams (0.017 m) of sebacoyl chloride and 200 grams of N-methyl-2- pyrrolidone. Methyl eosin (Solvent Red 44) (23.25 grams, 0.034 m) is added into the flask. The resulting mixture is stirred for one hour at ambient temperature, and then poured into distilled water. The product precipitate is filtered, washed with water, and dried at 750C and 0.1 Torr to obtain 23.25 grams of red monomer with a melting point range from 232.2° to 2370C. The solid is insoluble at 10% in hot HFIP, partially soluble at 10% in NMP, soluble in hot NMP, soluble at 10% in DMSO, and insoluble in hot ethanol.

EXAMPT,E VI Bis(methyl sebacate) of 4-(4-nltrophenylazo!reqorclnol (yellow) In a 500 ml three-necked flask equipped with nitrogen inlet and outlet, thermometer, condenser and mechanical stirrer, are placed 38.88 grams of 4-(4- nitrophenylazo)resorcinol (0.15 m), 24 grams of 50% NaOH solution, and 200 grams of N-methyl-2-pyrrolidone.

The resulting mixture is stirred at ambient temperature for 30 minutes. To 71.742 grams (0.3 m) of sebacoyl chloride in 500 ml of N-methyl-2-pyrrolidone is added 16.21 grams of sodium methoxide (0.3 m). The resulting solution is stirred for 30 minutes, and then is added into the flask with fast agitation. The reaction mixture is stirred for one hour at ambient temperature, and then poured into distilled water. The product precipitate is filtered, washed with water, and dried at 750C and 0.1 Torr to obtain 47.87 grams of yellow monomer with a melting point range from 1010 to 1080C.

The solid is insoluble at 10% in hot HFIP, soluble at

10% in NMP or DMSO, partially soluble at 10% in ethanol, and soluble in hot ethanol.

EXAMPLE VIT Bis(methyl sebacamide) of 9,9-dlmethyNqlllnacridone (magenta) In a one liter three-necked flask equipped with nitrogen inlet and outlet, thermometer, condenser and mechanical stirrer, are placed 35.63 grams of 2,9- dimethylquinacridone (0.1046 m), and 100 grams of N- methyl-2-pyrrolidone. The resulting mixture is stirred at ambient temperature for 30 minutes. To 50 grams (0.2091 m) of sebacoyl chloride in 400 ml of N-methyl- 2-pyrrolidone, is added 11.29 grams of sodium methoxide (0.2091 m). The resulting solution is stirred for 30

minutes and then added into the flask with fast agitation. The reaction mixture is stirred for one hour at ambient temperature, heated for 2 hours at 1000C, and then poured into distilled water (5 1) . The product precipitate is filtered, washed with water, and dried at 750C and 0.1 Torr to obtain 63.2 grams of magenta monomer with a melting point range from 135° to 1600C.

Following the procedures described in Examples I-VII, corresponding dye monomers are prepared with each of adipoyl chloride, isophthaloyl chloride and terephthaloyl chloride employed in place of sebacoyl chloride.

EXAMPLE VIII R1 .s (R-hvdroxv-9-methvlpropvl) terephthalate In a 2 liter three-necked flask equipped with nitrogen inlet and outlet, thermometer, condenser and mechanical stirrer, are placed 776.1 grams (4 m) of dimethyl terephthalate, 828 grams (9.2 m) of 2-methyl- 1,3-propanediol and 0.6936 grams of titanium tetraisopropoxide. The mixture is heated at 210EC for

2.5 hours while distilling out methanol. The reaction temperature is raised to 2500C, and excess 2-methyl- 1,3-propanediol is distilled off. The resulting product is cooled to room temperature, and recrystallized from methanol to provide 1091 grams of terephthalate diol monomer.

In a similar manner, 1,2-propanediol is employed as the alcohol reactant to produce bis(2-hydroxypropyl) terephthalate.

EXAMPLE IX Bis(2-tetradecyl-2-hydroxyethyl) terephthalate In a one liter three-necked resin flask equipped with nitrogen inlet and outlet, thermometer, condenser and mechanical stirrer, are placed 97.1 grams (0.5 m) of dimethyl terephthalate, 258.45 grams (1 m) of 1,2-hexadecanediol and 0.0865 grams of titanium tetraisopropoxide. The mixture is heated at 2100C for 2.5 hours while distilling out methanol. The reaction

temperature is raised and held at 2500C for 0.5 hour.

The resulting product is cooled to room temperature to provide a quantitative yield of terephthalate diol.

In a similar manner, 1,2-octanediol is employed as a reactant to obtain bis(2-hexyl-2- hydroxyethyl) terephthalate.

EX4MPTE X Polyester dye of polymerized yellow bis(3-hydroxy-2-methylpropyl) terephthalate of 2,2'-[(3,3'-dichloro-1,1'-diphenyl)-4,4'-bis(azo)]- <BR> <BR> <BR> <BR> bis TN- (2-methoxvhenvl) 1 -3-oxobutanamide where x/y is 98.66/1.34 mole percent.

In a one liter three-necked resin flask equipped with nitrogen inlet and outlet, thermometer, condenser and mechanical stirrer, are placed 200 grams

(0.604 m) of bis(3-hydroxy-2-methylpropyl) terephthalate and 6 grams of 2,2'-[(3,3'-dichloro-l,l'- diphenyl)-4,4'-bis(azo)]-bis[N-(2-methoxyphenyl)]-3- oxobutanamide (C.I. Pigment Yellow 17). The resulting mixture is heated to 2100C under vacuum, and the polymerization temperature is maintained for 3 hours.

The resulting polymer is cooled to room temperature to obtain yellow copolyester with a weight average molecular weight of 23,200 and number average molecular weight of 8400, a polydispersity of 2.8, a glass transition temperature of 490C, a heat of fusion of 0 j/g, a softening at about 100"C, a melt-viscosity of 1220 poises at 1500C, and a melt index of 110 g/10 min. at 1500C under a load of 2.16 Kg.

The polyester mixture is pulverized to an average particle size of about 5-7 microns suitable for electrophotographic imaging systems.

The procedure is repeated, except that the polymerization temperature is 240"C.

The polyester dye product has a weight average molecular weight of 33,000 and number average molecular weight of 10,800, a polydispersity of 3.1, a glass transition temperature of 530C, a heat of fusion of 0 j/g, a softening at about 100"C, a melt-viscosity of 7020 poises at 1500C, and a melt index of 19 g/10 min. at 1500C under a load of 2.16 Kg.

The polyester mixture is pulverized to an average particle size of about 5-7 microns.

EXAMPLE XI Polyester dye of polymerized yellow bis (2-hydroxypropyl) terephthalate of <BR> <BR> 2,2'-[(3,3'-dichloro-1,1'-diphenyl)-4,4'-bis(azo)]- bisUN-(9-methoxvphenvl)l-3-owoblltanamide where x/y is 99.64/0.36 mole percent.

In a one liter three-necked resin flask equipped with nitrogen inlet and outlet, thermometer, condenser and mechanical stirrer, are placed 193.49 grams (0.9964 m) of dimethyl terephthalate, 175.04 grams (2.3 m) of 1,2-propanediol, and 2.48 grams (0.0036 m) of 2,2'-L3,3'-dichloro-l,l'-diphenyl)-4,4'- bis(azo)]-bis[N-(2-methoxyphenyl)]-3-oxobutanamide (C.I. Pigment Yellow 17). The resulting mixture is heated to 2100C for 2 hours, at 2400C for 30 minutes,

and then at 2100C for 3 hours at 1 Torr. The resulting polymer is cooled to room temperature to obtain yellow copolyester with a weight average molecular weight of 10,000 and number average molecular weight of 4600, a polydispersity of 2.1, a glass transition temperature of 75"C, a heat of fusion of 0 j/g, a softening temperature at about 1300C, a melt-viscosity of 832 poises at 1500C, and a melt index of 160 g/10 min. at 1500C under a load of 2.16 Kg.

The copolyester is pulverized to an average particle size of 5-7 microns suitable for electrophotographic imaging systems.

EXAMPTE XTT Polyester dye of copolymerized bis(2-hydroxypropyl) terephthalate, bis (hydroxyethyl) terephthalate and yellow <BR> <BR> <BR> 2,2'-[3,3'-dichloro-l,l'-diphenyl)-4,4'-bis(azo)]- <BR> <BR> <BR> <BR> bis[N-(2-methoxyphenyl)]-3-oxobutanamide where x/y/z is 39.66/60/0.35 mole percent.

In a one liter three-necked resin flask equipped with nitrogen inlet and outlet, thermometer, condenser and mechanical stirrer, are placed 169.37 grams (0.6 m) of bis(2-hydroxypropyl) terephthalate, 100.83 grams (0.3966 m) of bis(hydroxyethyl) terephthalate, 2.5 grams (0.0036 m) of 2,2'-[(3,3'- dichloro-1,1'-diphenyl]-4,4'-bis(azo)]-bis[N-(2- methoxyphenyl)] -3-oxo-butanamide (C.I. Pigment Yellow 17), and 0.07 grams of titanium tetraisopropoxide. The resulting mixture is heated to 2100C for 30 minutes, and then vacuum is applied. The polymerization temperature is maintained at that temperature for 2 hours. The resulting polymer is cooled to room temperature to obtain yellow copolyester with a weight average molecular weight of 7300 and number average molecular weight of 3400, a polydispersity of 2.1, a glass transition temperature of 63"C, a heat of fusion of 0 j/g, a softening temperature range of 1000- 1300C, a melt-viscosity of 377 poises at 1500C, and a melt index of 360 g/10 min. at 1500C under a load of 2.16 Kg.

The copolyester is pulverized to an average particle size of 5-7 microns suitable for electrophotographic imaging systems.

EXAMPT XTTT Polyester dye of copolymerized bis(3-hydroxy-2-methylpropyl) terephthalate, bis(hydroxyethyl) terephthalate and yellow <BR> <BR> <BR> <BR> 2,2'-[(3,3'-dichloro-l,l'-diphenyl)-4,4'-bis(azo)]- <BR> <BR> <BR> <BR> <BR> <BR> <BR> bis[N-(2-methoxyphenyl)]-3-oxobutanamide. where x/y/z is 64.66/35/0.34 mole percent.

In a one liter three-necked resin flask equipped with nitrogen inlet and outlet, thermometer,

condenser and mechanical stirrer, are placed 108.62 grams (0.35 m) of bis(3-hydroxy-2-methylpropyl) terephthalate, 164.39 grams (0.6466 m) of bis(hydroxyethyl) terephthalate, 2.5 grams (0.0034 m) of 2,2'-[(3,3'-dichloro-1,1'-diphenyl)-4,4'-bis(azo)]- bis[N-(2-methoxyphenyl)]-3-oxo-butanamide (C.I. Pigment Yellow 17), and 0.12 grams of titanium tetraisopropoxide. The resulting mixture is heated to 210EC for 30 minutes, and then vacuum is applied. The polymerization temperature is maintained at that temperature for 45 minutes. The resulting polymer is cooled to room temperature to obtain yellow copolyester with a weight average molecular weight of 14,000 and number average molecular weight of 6400, a polydispersity of 2.2, a glass transition temperature of 530C, a heat of fusion of 0 j/g, a softening temperature at about 115"-120"C, a melt-viscosity of 620 poises at 1500C, and a melt index of 220 g/10 min. at 1500C under a load of 2.16 Kg.

The above copolyester is pulverized to an average particle size of 5-7 microns suitable for electrophotographic imaging systems.

EXAMPLE XIV Polyester dye of copolymerized bis(3-hydroxy-2-methylpropyl) terephthalate, bis(hydroxyethyl) terephthalate and yellow <BR> <BR> <BR> 2,2'-[(3,3'-dichloro-1,1'-diphenyl)-4,4'-bis(azo)]- <BR> <BR> <BR> bis[N-(2-methoxyphenyl)]-3-oxobutanamide. where x/y/z is 49.83/49.83/0.34 mole percent.

In a one liter three-necked resin flask equipped with nitrogen inlet and outlet, thermometer,

condenser and mechanical stirrer, are placed 154.65 grams (0.4983 m) of bis(3-hydroxy-2-methylpropyl) terephthalate, 126.68 grams (0.4983 m) of bis(hydroxyethyl) terephthalate, 2.5 grams (0.0034 m) of 2,2'-[(3,3'-dichloro-1,1'-biphenyl)-4,4'-bis(azo)]- bis[N-(2-methoxyphenyl)]-3-oxo-butanamide(C.I. Pigment Yellow 17), and 0.09 grams of titanium tetraisopropoxide. The resulting mixture is heated to 2100C for 30 minutes, and then vacuum is applied. The polymerization temperature is maintained at that temperature for one hour. The resulting polymer is cooled to room temperature to obtain yellow copolyester with a weight average molecular weight of 23,000 and number average molecular weight of 9000, a polydispersity of 2.6, a glass transition temperature of 550C, a heat of fusion of 0 j/g, 3090 poises at 1500C, and a melt index of 44 g/10 min. at 1500C under a load of 2.16 Kg.

The above copolyester is pulverized to an average particle size of 5-7 microns suitable for electrophotographic imaging systems.

EXAMPLE XV Polyester dye of polymerized magenta bis(3-hydroxy-2-methylpropyl) terephthalamide of 2,9-dimethylquinacridone where x/y is 98.65/1.35 mole percent.

In a one liter three-necked resin flask equipped with nitrogen inlet and outlet, thermometer, condenser and mechanical stirrer, are placed 200 grams (0.6403 m) of bis(3-hydroxy-2-methylpropyl) terephthalate and 3 grams (0.088 m) of 2,9- dimethylquinacridone. The resulting mixture is heated to 2250C under vacuum, and the polymerization

temperature is maintained for 3 hours. The resulting polymer is cooled to room temperature to obtain magenta copolyester with a weight average molecular weight of 29,800 and number average molecular weight of 10,000, a polydispersity of 3.0, a glass transition temperature of 520C, a heat of fusion of 0 j/g, a softening at about 100"C, a melt-viscosity of 3170 poises at 1500C, and a melt index of 43 g/10 min. at 1500C under a load of 2.16 Kg.

The polyester mixture is pulverized to an average particle size of about 5-7 microns.

EXAMPLE XVI Polyester dye of copolymerized bis(3-hydroxy-2-methylpropyl) terephthalate, bis (hydroxyethyl) terephthalate and magenta bls(methv1 sebacamide) o 9, . 9-dmetThyraorc1one

where x/y/z is 68.58/29.57/1.85 mole percent.

In a one liter three-necked resin flask equipped with nitrogen inlet and outlet, thermometer, condenser and mechanical stirrer, are placed 59.97 grams (0.1932 m) of bis(3-hydroxy-2-methylpropyl) terephthalate, 113.95 grams (0.4482 m) of bis(hydroxyethyl) terephthalate, 8.92 grams of bis(methyl sebacamide) of 2,9-dimethylquinacridone, and 0.1021 grams of titanium tetraisopropoxide. The resulting mixture is heated to 2250C under vacuum, and the polymerization temperature is maintained for 3 hours. The resulting polymer is cooled to room temperature to obtain magenta copolyester with a weight average molecular weight of 35,000 and number average molecular weight of 12,000, a polydispersity of 2.9, a glass transition temperature of 620C, a heat of fusion of 0 j/g, a softening at about 145"C, a melt-viscosity of 188,000 poises at 1500C, and a melt index of 0.72 g/10 min. at 1500C under a load of 2.16 Kg.

The copolyester mixture is pulverized to an average particle size of about 5-7 microns.

The procedure is repeated, except that x/y/z is 49.075/49.075/1.85. The copolyester has a weight average molecular weight of 46,000 and a number average molecular weight of 19,000, a polydispersity of 2.4, a glass transition temperature of 590C, a heat of fusion of 0 j/g, a softening at about 1350C, a melt-viscosity of 8500 poises at 1500C, and a melt index of 1.6 g/10 min. at 1500C under a load of 2.16 Kg.

EXAMPLE XVII Polyester dye of bis(3-hydroxy-2-methylpropyl) terephthalate and magenta bis(methyl sebacamide) of 9 9-dimethvlaulnacridone where y/z is 98.15/1.85 mole percent.

In a one liter three-necked resin flask equipped with nitrogen inlet and outlet, thermometer, condenser and mechanical stirrer, are placed 200 grams (0.64 m) of bis(3-hydroxy-2-methylpropyl) terephthalate and 8.92 grams (0.0121 m) of bis(methyl sebacamide) of 2,9-dimethylquinacridone. The resulting mixture is heated to 2250C under vacuum, and the polymerization temperature is maintained for 3 hours. The resulting polymer is cooled to room temperature to obtain magenta copolyester with a weight average molecular weight of 20,000 and number average molecular weight 7700, a polydispersity of 2.6, a glass transition temperature of 44"C, a heat of fusion of 0 j/g, a softening at about 135"C, a melt-viscosity of 719 poises at 1500C, and a melt index of 190 g/10 min. at 1500C under a load of 2.16 Kg.

The polyester mixture is pulverized to an average particle size of about 5-7 microns.

EXAMPTE XVTTT Polyester dye of copolymerized bis(3-hydroxy-2- methylpropyl) terephthalate, bis (hydroxyethyl) terephthalate, bis(2-tetradecyl-2-hydroxyethyl) terephthalate and magenta bis(methyl sebacamide) of 2,9-dimethylquinacridone where R is C1,-H2,, and x/y/z/w is 68.18/29.22/0.8/1.8 mole percent.

In a one liter three-necked resin flask equipped with nitrogen inlet and outlet, thermometer, condenser and mechanical stirrer, are placed 59.97 grams (0.192 m) of bis(3-hydroxy-2-methylpropyl) terephthalate, 113.95 grams (0.4482 m) of bis(hydroxyethyl) terephthalate, 8.92 grams (0.0121) of bis (methyl sebacamide) of 2,9-dimethyl-quinacridone, 3.478 grams (0.0054 m) of bis(2-tetradecyl-2- hydroxyethyl) terephthalate, and 0.1021 grams of titanium tetraisopropoxide. The resulting mixture is heated to 2250C under vacuum, and the polymerization temperature is maintained for 3 hours. The resulting polymer is cooled to room temperature to obtain magenta copolyester with a weight average molecular weight of 17,000 and number average molecular weight of 7600, a polydispersity of 2.2, a glass transition temperature of 52"C, a heat of fusion of 0 j/g, a softening at about 115"C, a melt-viscosity of 2280 poises at 1500C, and a melt index of 59 g/10 min. at 1500C under a load of 2.16 Kg.

The copolyester mixture is pulverized to an average particle size of about 5-7 microns.