GB2353533A

GB2353533A - Ink jet dyes based on two aliphatically linked [7-(ortho-carboxyarylazo)-8-hydroxydisulphonaphth-2-ylamino]-(dia/tria)zinyl units

Info

Publication number: GB2353533A
Application number: GB0015905A
Authority: GB
Inventors: Paul Wight; Julie Ann Stocks
Original assignee: Avecia Ltd
Current assignee: Avecia Ltd
Priority date: 1999-07-10
Filing date: 2000-06-29
Publication date: 2001-02-28
Anticipated expiration: 2020-06-29
Also published as: GB2353533B; GB9916110D0; GB0015905D0; US6506241B1

Abstract

Compounds of the Formula (1) and salts thereof: <EMI ID=1.1 HE=59 WI=124 LX=427 LY=525 TI=CF> <PC>wherein:<BR> <DL TSIZE=18> <DT>each A<DD>independently is N, C-Cl, C-CN or C-NO<SB>2</SB>; <DT>each Ar<DD>independently is a substituted aryl group carrying a -COOH group ortho to the azo (-N=N-) group; <DT>L<DD>is an aliphatic group carrying a -COOH, -SO<SB>3</SB>H or -PO<SB>3</SB>H<SB>2</SB> group; <DT>each Z<DD>independently is -SR<SP>2</SP>, -OR<SP>3</SP>, -NR<SP>4</SP>R<SP>5</SP> or a labile atom or group; <DT>each X<DD>independently is -S-, -O- or -NR<SP>1</SP>-; <DT>each R<SP>1</SP><DD>independently is H or optionally substituted alkyl; and <DT>R<SP>2</SP>, R<SP>3</SP>, R<SP>4</SP> and R<SP>5</SP><DD>are independently H, optionally substituted alkyl, optionally substituted aryl or optionally substituted aralkyl; or <DT>R<SP>4</SP> and R<SP>5</SP><DD>together with the nitrogen to which they are attached form an optionally substituted five or six membered ring, are magenta dyes that are highly soluble in aqueous media, have good light-fastness and may be incorporated into inks for ink jet printing. </DL> L may be interrupted by oxygen, sulphur, nitrogen, carbonyl (C=O) or a combination thereof. L may be optionally unsaturated and/or further substituted. When Z is a labile atom or group, it is preferably an atom or group which is displaceable by a hydroxyl group of cellulose under mildly alkaline aqueous conditions to form a covalent bond between the dye of Formula (1) and cellulose. Z may include halogen atoms, for example F or Cl; sulphonic acid groups; thiocyano groups; quaternary ammonium groups, for example trialkylammonium groups and optionally substituted pyridinium groups, for example 3- and 4-carboxy pyridinium groups. Also claimed are compositions and inks containing a compound of Formula (1), a process for ink jet printing using the inks and an ink jet printer cartridge containing the ink.

Description

2353533 COMPOUNDS AND INKS This invention relates to compositions, to inks

and to dyes and to their use in ink jet printing ("IJP").

UP is a non-impact printing technique in which droplets of ink are ejected through a fine nozzle onto a substrate without bringing the nozzle into contact with the substrate.

There are many demanding performance requirements for dyes in inks used in UP. For example they desirably provide sharp, non-feathered images having good water-fastness, light-fastness and optical density. The inks are often required to dry quickly when applied to a substrate to prevent smudging, but they should not form a crust over the tip of an ink jet nozzle because this will stop the printer from working. The inks should also be stable to storage over time without decomposing or forming a precipitate which could block the fine nozzle.

According to the first aspect of the present invention there is provided a compound of the Formula (1) and salts thereof:

1 N 1, N N Z N R \ 'J'I 1 OH N A X-L- A _)" N R OH Ar-N=N N=N-Ar H 03S S03H S03H&SO3H Formula (1) wherein:

each A independently is N, C-Cl, C-CN or C-N02, each Ar independently is a substituted aryl group carrying a -COOH group ortho to the azo (-N=N-) group; L is an aliphatic group carrying a -COOH, -SO3H or-p03H2group; each Z independently is -SR 2, -OR 3, -NR'R 5 or a labile atom or group; each X independently is -S-, -0- or -NR'-; each R1 independently is H or optionally substituted alkyl; and R 2, R 3, R' and R' are each independently H, optionally substituted alkyl, optionally substituted aryl or optionally substituted aralkyl; or Wand R 5 together with the nitrogen to which they are attached form an optionally substituted five or six membered ring.

Preferably each A is N.

2 Preferably the aryl groups represented by Ar contain up to 12 carbon atoms, more preferably up to 10 carbon atoms and optionally contain one or more hetero atoms selected from 0, S and N. The aryl groups optionally carry one or more substituents in addition to the -COOH group ortho to the azo group in Formula (1).

Suitable aryl groups containing one or more heterc, atoms include pyridyl, pyrazolyl, thienyl or indanyl. It is preferred however that the aryl groups are free from hetero atoms, for example phenyl or naphthyl.

More preferably each Ar independently is optionally substituted 1-carboxynaphth-2-yl or optionally substituted 2-carboxy phenyl. It is especially preferred that each Air independently is of the Formula (2) or (3):

COOH COOH (E3)n Formula (2) Formula (3) wherein: each B independently is -OH, -S03H, -P031-12, -COOH, -CF3, optionally substituted alky], is optionally substituted alkoxy, optionally substituted amino, halo, - N02, -CN or -S02T; T is optionally substituted alkyl (preferably optionally substituted C,,)- alkyl) optionally substituted aryl (preferably optionally substituted phenyl), - NIR'R', vinyl or a group convertible to vinyl on treatment with aqueous alkali; R' and R' are each, independently, H, optionally substituted alkyl or optionally substituted aryl, or R 6 and R7 together with the nitrogen to which they are attached form an optionally substituted piperazinyl, morphoiinyl or piperidinyl ring; n is 0 to 6; and p is 0 to 4.

Preferably R' and R 7 are each independently H, optionally substituted C,, -alkyl or optionally substituted phenyl, more preferably H, optionally substituted C,-6-alkyl or optionally substituted phenyl.

When T is a group which is convertible to vinyl on treatment with aqueous alkali it is preferably of the formula -CH2CH2OS0,1-1, -CH2CH2SSO3H, -CH2CH2C1 or -CH2CH20COCH, Preferably T is -NR'R', -CH=CH2 or -CH2CH2OSO,H and especially -CH=CH2or -NR'R', wherein R' and R' are as hereinbefore defined.

Preferably each B independently is -COOH, -S03H, -PO,H2, -CF, optionally substituted C,-10-alkoxy, optionally substituted C,,O-alkyl, optionally substituted amino 3 -S02CH=CH2, -Cl, -Br, -1, -CN, -OH, -N02 or -S02NR'R', wherein R6 and R 7 are as hereinbefore defined.

Preferred optional substituents on B are selected from Cl-6-alky], C,,hydroxyalkyl, C,-alkoxy, C,-alkylCO, -OH, -S03H, -COOH, -CN, -P03H2, halo and -NH2.

In a preferred embodiment each B independently is -COOH, -S03H, -OH, -CF3, C1v -NH2, -NHCOC1,4kyl, -NHC,,-alkyl, -NHC,,-hydroxyalkyi, Cl-65-alkoxy S02NI-IC1-4-alkyl, -S02NHC,-4-hydroxyalkyl or C,-6-alkyl optionally substituted by -OH, - COOH, -NH2 or -S03H. It is especially preferred that each B independently is Cl-4-alkyl, -COOH, -OH, -SO,H or -NI-ICOC1,-alky], more especially methyl, ethyl, -NHCOCH, or - COOH.

Preferably any substituents represented by B in Formulae (2) and (3) are located in a position other than the ortho position relative to the azo group in Formula (1).

Preferably each n independently is 0, 1 or 2, more preferably 0.

Preferably each p independently is 0, 1 or 2, more preferably 0.

In a preferred embodiment each Ar is, independently, of the Formula (3) wherein is each p is 0, 1 or 2 (preferably 0) and each B is as hereinbefore defined, more preferably -COOH, -OH, -S03H or -Cl. It is especially preferred that each Ar is 2- carboxypheny].

For ease of synthesis it is preferred that each Ar is the same.

Preferably each R' independently is H or optionally substituted C,-Calkyl, more preferably H or Cl-4-alkyl optionally substituted by -COOH, -S03H, -CN or more preferably -OH. It is especially preferred that each R' independently is H, methyl, ethyl or hydroxyethyl. It is most preferred that each R' is H.

Preferably each X independently is -S- or -NR'-, more preferably -NR'- and especially -NH-.

When R 2, R', R' or R5 is optionally substituted alkyl it is preferably optionally substituted Cl-M-alkyl, more preferably optionally substituted Cl,O-alkyl and especially optionally substituted Cl_.-alkyl. Preferred optional substituents, include Cl,,-alkoxy, Cl-6-hydroxyalkoxy, -OH, -COOH, -S03H, -P03H2, -CN, a 5- or 6- membered heterocyclic group or optionally substituted amino. Preferred 5- or 6- membered heterocyclic groups are furanyl, tetrahydrofurany], piperazinyl and morpholinyl each of which is optionally substituted by -OH, -COOH, -SO3H or C,,-alkyl.

When any of R 2, R 3, R' or R5 is optionally substituted aryl it is preferably optionally substituted phenyl or naphthyl, more preferably optionally substituted phenyl. Preferred optional substituents are Cl,,,-alkoxy, halo (preferably F or Cl), -OH, - CN, -COOH, -S03H, -P03H2, -N02l -NH2, -COC1-4-alkyl, -NI-ICOC,-4-alkyl -(C,,,>-alkylene)O(C, -, alkylene)OC,-4-alkyi, -(C2-6-alkylene)O(C2-,-alkylene)OH, -S02NH2, S02NHC,,-alkyi, Cl-6-alkyl or Cl-,- alkyl substituted by -OH, -COOH or -S03H.

Examples of aryl groups which may be represented by any of R 2, R3, R 4 or R5 include 2-sulphopheny], 2-carboxyphenyl, 4-sulphophenyl, 4-carboxyphenyl, 2-carboxy-4- 4 sulphophenyl, 3-carboxy-2-methyl-phenyl, 4-methyi-3-sulpho-phenyl or 2, 6dimethylphenyl.

When any of R 2, R 3, R 4 or R5 is optionally substituted aralkyl it is preferably of the formula:

-(C,-,-alkylene)-G (R 8) wherein each R' independently is C,-4-alkyl, Cl,-alkoxy, halo, -OH, -NH2, -COOH, - SO,H or -P03H2; and a is 0 to 5.

a is preferably 0, 1 or 2.

Especially preferred aralkyl groups which may be represented by R 2, R 3, R 4 or R5 are benzyl or 2-phenylethy], each of which is optionally substituted by - COOH, -OH or -SO,H.

When R 4 and R5 together with the nitrogen to which they are attached form an is optionally substituted 5 or 6 membered ring it is preferably an optionally substituted piperazinyl, piperidinyl or morpholinyl ring. The optional substituents on the ring are preferably selected from -OH, -COOH, -SO,H, C,-alkoxy, C,-alkyl and C,- alkyl substituted by -OH, -COOH or -S03H.

When Z is a labile atom or group, it is preferably an atom or group which is displaceable by a hydroxyl group of cellulose under mildly alkaline aqueous conditions to form a covalent bond between the dye of Formula (1) and cellulose.

Preferred labile atoms and groups which may be represented by Z include halogen atoms, for example F or Cl; sulphonic acid groups; thiocyano groups; quaternary ammonium groups, for example triaikylammonium groups and optionally substituted pyridinium groups, for example 3- and 4-carboxy pyridinium groups. An especially preferred labile atom is Cl.

It is preferred, however, that each Z independently is -SR 2, -OR' or -NR 4 R', more preferably -OH, -SR 2 or -NR 4 R' wherein R 2, R 4 and R' are as hereinbefore defined. It is especially preferred that each Z independently is -OH, -SH or -NIR'R wherein R' and R each independently is H, C,,-alkyl optionally substituted by -OH, Cl-4- alkoxy, C,,-hydroxyalkoxy, -COOH or -SO,H. Most preferably each Z independently is -OH, -SH or -NH2.

The floating -S03H groups in Formula (1) are preferably attached at the 4or, more preferably, the 3- position on the naphthylene groups in Formula (1) relative to the -NR'- group.

L preferably contains less than 20, more preferably less than 10 carbon atoms. L may contain one or more hetero atoms, for example oxygen, nitrogen or sulphur, or a combination thereof. For example, L may contain an ester, amide or -SS- group. L may be linear or branched but is preferably linear. L may be unsaturated or, more preferably, saturated.

Preferably L is an optionally interrupted alkenylene group or more preferably an optionally interrupted alkylene group containing up to 20, more preferably up to 10 carbon atoms, said group carrying a substituent selected from -COOH, -S03H and - P03H2.

When L is alkylene it is preferably optionally interrupted C2-20-, more preferably C2-10- and especially C2-6-alkylene which carries a substituent selected from -COOH, -S03H and -P03H2. When L is interrupted alkylene or alkenylene the interruption(s) islare preferably one or more hetero, atoms, preferably -0-, -S-, -SS- or -NR'- wherein R' is as hereinbefore defined.

It is especially preferred that L is a straight chain C2-Calkylene group optionally interrupted by one or more -SS- group, wherein the alkylene group carries a substituent selected from -COOH, -S03H and -P03H2.

is L may carry more than one substituent selected from -COOH, -SO.H and P03H2, or other substituents in addition those selected from -COOH, -S03H and - P03H2, for example -OH. However, it is preferred that the substituents on L are selected from the group consisting of -COOH, -S03H and P03H2. More preferably L is substituted by one or more -S031-1 or -COOH group. It especially preferred that L is substituted by one or more -COOH group.

Examples of preferred aliphatic groups represented by L include -CH(COOH)CH2-S-S-CH2CH(COOH)-, -CH2CH(COOH)CH2- and -CH2CH2CH2CH(COOH)-.

The compounds of Formula (1) may exist in tautomeric forms other than those shown in this specification, for example the hydrazo tautomer. These tautomers are included within the scope of the present claims.

The compounds of Formula (1) have a high solubility in aqueous media and provide bright magenta prints with a good light-fastness when incorporated into inks for inkjet printing.

In view of the foregoing preferences, preferred compounds of the Formula (1) are of Formula (4) and salts thereof:

Z1 Z1 N'-N N"N COOH R 11 R 11 COOH 1 OH N'JI'N;NR" L' NR"1,. N OH N.5 6N 11 N16 - N N" H03 S 1 S03H H03S"" SO3H Formula (4) 6 wherein:

L' is a C,o-alkylene group carrying a -SO,H or -COOH group; each R independently is H or C,-alkyl optionally substituted by -OH, - COOH, -SO,H or -CN; each Z' independently is -SR', -OR 3 or -NR 4 R 5; and R', R', R' and R' are as hereinbefore defined.

The compounds of Formula (4) exhibit a particularly high aqueous solubility and when incorporated into inks suitable for use in an ink jet printer, provide prints with a high light-fastness.

Preferably each R.' independently is H or C,,-alkyl optionally substituted by -OH.

More preferably each R" is H.

Preferably each Z' independently is -OH, -SH or -NR'R", wherein R' and R are as hereinbefore defined.

Preferably L' is a straight chainC2-1,-, more preferably aC2,-alkylene group which is carries a one or more substituents selected from -COOH and -S03H.

Especially preferred compounds of the Formula (4) are those wherein L' is C2-1,-alkylene carrying a -COOH group and each Z is -OH, -SH or -NR'R" (especially -NH2), wherein R' and R are as hereinbefore defined.

The compounds according to the first aspect of the invention may be in the free acid or salt form. Preferred salts are alkali metal salts, especially lithium, sodium and potassium salts, ammonium and substituted ammonium salts. Especially preferred salts are salts with sodium, lithium, ammonia and volatile amines and mixed salts thereof, especially mixed lithiumlsodium salts. The compounds may be converted into a salt using known techniques. For example, an alkali metal salt may be converted into a salt with ammonia or an amine by dissolving an alkali metal salt in water, acidifying with a mineral acid and adjusting the pH of the solution to pH 9 to 9.5 with ammonia or the amine and removing the alkali metal cations by dialysis, reverse osmosis or ultraffitration.

The compounds of the invention may be prepared using conventional techniques for the preparation of azo dyes. For example a suitable method comprises condensing a molar excess of the compound of the formula ZH with the compound of the Formula (5):

C] cl 1 N N N "J_" N 1 R\ 1,L R OH N A X-L-X A N OH Ar-N N-Ar N N m - "5, 1 1 H03S_. S03H S03H S03H Formula (5) 7 wherein L and each Z, Ar, R', X and A are as hereinbefore defined.

The condensation is preferably performed in a liquid medium, more preferably an aqueous medium and especially water. Temperatures of 101C to 1001C are preferred, more preferably from 20 to 950C. Preferably a reaction time of 1 to 24, more preferably 1 to 4 hours is used.

The condensation is preferably performed in the presence of a suitable base and optionally with a catalyst, for example 4-d i methyl aminopyrid i ne.

The base may be any inorganic base for example, ammonia, an alkali metal or alkali earth metal hydroxide, carbonate or bicarbonate, or an organic base. The amount of base used may be varied between wide limits but it is preferred to use less than 40, more preferably less than 10 and especially from 3 to 5 moles for each mole of the compound of Formula (5).

After the condensation reaction the product may be isolated by precipitating the is product as a salt from the reaction mixture for example by the addition of a suitable alkali metal salt, especially sodium chloride. Alternatively, the product may be isolated in its free acid form by acidifying the reaction mixture, preferably using a mineral acid, especially hydrochloric acid. Where the product precipitates as a solid it may be separated from the mixture by filtration.

If desired unwanted anions may be removed from the product of the above process by dialysis, osmosis, ultrafiltration or a combination thereof.

The product of the above process may be converted, if desired, to the NH4+ , quaternary ammonium or organic amine salt by the addition of ammonia, ammonium hydroxide, primary, secondary, tertiary or quaternary amine.

The compound of Formula (5) may, for example, be prepared as follows:

stacie (a):

diazotising amine of the formula Ar-NH2 and coupling with the compound of the Formula (6):

R\ OH NCOCH3 H03S S03H Formula (6) staqe (b) hydrolysis, under alkaline conditions, to remove the acetyl group present in the product of stage (a); stage (c) 8 condensing the product of stage (b) with an approximately molar equivalent of the compound of the Formula (7):

cl N'-N cl -21, A; Cl Formula (7) staqe( condensing a compound of the formula HX-L-XH with approximately 2 molar equivalents of the product of stage(c); wherein Ar, and R', A, L and X are as hereinbefore defined.

The diazotisation in stage (a) is preferably performed in an aqueous medium at a pH below 7 in the presence of a suitable diazotisation agent. Dilute mineral acid, e.g. HCI or H2S04, is preferably used to achieve the desired acidic conditions. Conveniently the diazotisation agent is formed in-situ, for example by dissolving an alkali metal nitrite, preferably sodium nitrite, in a molar excess of mineral acid, preferably HCL is The temperature of the diazotisation is not critical and may conveniently be carried out at from -5'1C to 200C, preferably from 0 to 1 OOC and especially from 0 to 50C.

The coupling reaction in stage (a) is preferably performed under mildly alkaline conditions, more preferably at a pH of 7-8.

The hydrolysis in stage (b) is preferably performed in aqueous NaOH at a reaction temperature of 50 to 900C.

The condensations in stages (c) and (d) are preferably performed in the presence ofa base.

The present invention also covers mixtures comprising two or more dyes of the Formula (1). Furthermore, the dyes of Formula (1) may be mixed with commercially available dyes, especially those listed in the colour Index International, to adjust the shade or other properties as desired.

According to a second aspect of the present invention there is provided a composition comprising:

(a) one or more compound of the Formula (1) according to the first aspect of the present invention; and (b) one or more water-soluble magenta dye other than a compound of Formula (1) according to the first aspect of the invention.

The water-soluble magenta dye is preferably a xanthene dye, an azo or bis azo dye, more preferably an anionic azo or bis azo dye and especially an azo or bis azo dye which contains one or more groups selected from sulphonate, carboxylate and thiocarboxylate groups.

9 Preferred water-soluble magenta dyes include C.I. Acid Red 50, 52, 87, 91, 92, 95, 249 and 289; C.I. Direct Violet 106 and 107; compounds 100 to 107, 200 and 201 described on pages 8 and 9 of W096124636; compounds 1 to 24 shown described on cols. 4 to 10 in US 5,542,970; compounds 1 to 55 described on pages 7 to 17 of EP-A-682 088; compounds 1 to 14 shown in Example 1 to 6 of EPAA94,885; compounds 1 to 24 described on pages 8 to 13 of EP-A-717 089; the compounds described in examples 1 to 16 in cols 5 to 11 of US 5,262,527; the dyes described in Examples 1 to 21 in WO 94/16021; and one or more dyes of the Formula (8) and salts thereof:

R 12 W NH2 N- N-- 11 N A- OH H03S Q H03S OH N A N NH 112 N- 2 v R W Formula (8) is wherein:

each v is independently, -S03H, -COOH, -CF3, alkoxy, alkyl or -P03H2; Q is an organic linking group; each R 12 is independently, H or optionally substituted alkyl; each A independently is N, C-Cl, C-CN or C-N02; each W is independently, -SR 13, -OR", -NRR or halogen; 13 14 R, R ' R15 & W' are, each independently, H, optionally substituted alkyl, optionally substituted aryl or optionally substituted aralkyl; or R 14 and R 15 together with the nitrogen to which they are attached, form an optionally substituted five or six membered ring; Especially preferred water-soluble magenta dyes for use in the composition according to the second aspect of the invention include C.L Acid Red 52, C.I. Acid Red 289 or a dye of the Formula (9), (10) and (11) and salts thereof: cl S03H OH NH--- N- N -NH N=N W H03S S03H -NH S03H 2 5 Formula (9) COOH 0 H OH NH- N HOOC" N=N W CH3 H03S S03H N N- 2 - -JC H Formula (10) N H 2 H 03S N', H OH '/- N CH 2 CH 2 0 H N N N CH CH OH H03S H03SCH 2 CH 2 NH /- 22 Formula (11) The dye of Formula (9) may be prepared using the method described in Example is 1 of EP 0 559 310. The dye of the Formula (10) may be prepared using the method described in Example 3 of PCT publication number WO 94/16021. The dye of Formula (11) may be prepared using the method described in Example 1 of WO 96124636.

The composition according to the second aspect of the present invention preferably comprises:

(a) from 1 to 99, more preferably from 3 to 70 and especially from 5 to 50 parts in total of the compound(s) of Formula (1); and 11 (b) from 99 to 1, more preferably from 30 to 97 parts and especially 95 to 50 parts in total of the water-soluble magenta dye(s); wherein the parts are by weight and the sum of the parts (a) + (b) = 100 The composition may contain a single dye of Formula (1) or a mixture of two or more dyes of the Formula (1). Similarly, the composition may contain a single water-soluble magenta dye other than a compound of Formula (1) or a mixture of two or more water-soluble magenta dyes other than compounds of Formula (1).

The compounds and compositions according to the first and second aspects of the present invention may be, and preferably are, purified to remove undesirable impurities before they are incorporated into inks for inkjet printing. Conventional techniques may be employed for purification, for example ultrafiltration, reverse osmosis andlor dialysis.

According to a third aspect of the present invention there is provided an ink comprising:

(a) a compound according to the first aspect of the present invention, or a is composition according to the second aspect of the invention; and (b) a liquid medium.

Preferably component (a) of the ink is one of the preferred compounds or compositions as hereinbefore described in relation to the first or second aspect of the invention. More preferably component (a) is one or more compounds of the Formula (1) or Formula (4), as hereinbefore defined.

The liquid medium preferably comprises:

(i) water; (ii) a mixture of water and an organic solvent; or (iii) an organic solvent free from water.

The number of parts by weight of component (a) of the ink is preferably from 0.01 to 30, more preferably 0.1 to 20, especially from 0.5 to 15, and more especially from 1 to 5 parts. The number of parts by weight of component (b) is preferably from 99.99 to 70, more preferably from 99.9 to 80, especially from 99.5 to 85,and more especially from 99 to 95 parts. The number of parts (a) + (b) is 100.

Preferably component (a) is completely dissolved in component (b). Preferably component (a) has a solubility in component (b) at 200C of at least 10%. This allows the preparation of concentrates which may be used to prepare more dilute inks and reduces the chance of the compound(s) of component (a) of the ink precipitating if evaporation of the liquid medium occurs during storage.

When the liquid medium comprises a mixture of water and an organic solvent, the weight ratio of water to organic solvent is preferably from 99:1 to 1:99, more preferably from 99:1 to 50:50 and especially from 95:5 to 80:20.

It is preferred that the organic solvent present in the mixture of water and organic solvent is a water-miscible organic solvent or a mixture of such solvents. Preferred 12 water-miscible organic solvents include Cl-,-alkanols, preferably methanol, ethanol, n-propanol, isopropanol, n-butanol, sec-butanol, tert-butanol, n-pentanol, cyclopentanol and cyclohexanol; linear amides, preferably dimethylformamicle or dimethylacetamide; ketones and ketone-alcohols, preferably acetone, methyl ether ketone, cyclohexanone and diacetone alcohol; water-miscible ethers, preferably tetrahydrofuran and dioxane; diols, preferably diols having from 2 to 12 carbon atoms, for example pentane-1, 5-diol, ethylene glycol, propylene glycol, butylene glycol, pentylene glycol, hexylene glycol and thiodiglycol and oligo- and poly-alkyleneglycols, preferably diethylene glycol, triethylene glycol, polyethylene glycol and polypropylene glycol; triols, preferably glycerol and 1,2,6-hexanetriol; mono-C,,-alkyl ethers of diols, preferably mono-C,,- alkyl ethers of diols having 2 to 12 carbon atoms, especially 2-methoxyethanol, 2-(2- methoxyethoxy)ethanol, 2-(2-ethoxyethoxy)-ethanol, 2-[2-(2-methoxyethoxy)ethoxy]ethanol, 2-[2-(2-ethoxyethoxy)-ethoxy]-ethanoI and ethyleneglycol monoallylether; cyclic amides, preferably 2-pyrrolidone, N-methyl-2-pyrrolidone, N-ethyl-2-pyrrolidone, caprolactarn and 1,3-dimethylimidazolidone; cyclic esters, preferably caprolactone; sulphoxides, preferably dimethyl sulphoxide and sulpholane. Preferably the liquid medium comprises water and 2 or more, especially from 2 to 8, water-miscible organic solvents.

Examples of further suitable ink media comprising a mixture of water and one or more organic solvents are described in US 4,963,189, US 4,703,113, US 4, 626,284, EP 425,150A and US 5,207,824.

When the liquid medium comprises an organic solvent free from water, (i.e. less than 1 % water by weight) the solvent preferably has a boiling point of from 300 to 200"C, more preferably of from 400 to 1500C, especially from 50 to 125"C. The organic solvent may be water-i m miscible, water-miscible or a mixture of such solvents. Preferred water-miscible organic solvents are any of the hereinbefore described water-miscible organic solvents and mixtures thereof. Preferred water-immiscible solvents include, for example, aliphatic hydrocarbons; esters, preferably ethyl acetate; chlorinated hydrocarbons, preferably CH2CI2; and ethers, preferably diethyl ether; and mixtures thereof.

When the liquid medium comprises a water-immiscible organic solvent, preferably a polar solvent is included because this enhances solubility of the dye in the liquid medium. Examples of polar solvents include C,,-alcohols. In view of the foregoing preferences it is especially preferred that where the liquid medium is an organic solvent free from water it comprises a ketone (especially methyl ethyl ketone) Wor an alcohol (especially a C,,-alkanol, such as ethanol or propanol).

The organic solvent free from water may be a single organic solvent or a mixture of two or more organic solvents. It is preferred that when the medium is an organic solvent free from water it is a mixture of 2 to 5 different organic solvents. This allows a 13 medium to be selected which gives good control over the drying characteristics and storage stability of the ink.

Ink media comprising an organic solvent free from water are particularly useful where fast drying times are required and particularly when printing onto hydrophobic and s non-absorbent substrates, for example plastics, metal and glass.

An especially preferred ink comprises:

(a) from 1 to 10 parts in total of a compound or composition according to the first or second aspect of the invention; (b) from 2 to 60, more preferably 5 to 40 parts of water-soluble organic solvent; and (c) from 30 to 97, more preferably 40 to 85 parts water; wherein all parts are by weight and the sum of the parts (a) + (b) + (c) = 100.

The ink may also contain additional components conventionally used in ink jet printing inks, for example viscosity and surface tension modifiers, corrosion inhibitors, biocides, kogation reducing additives, anti-cockle agents to reduce paper curling and is surfactants which may be ionic or non-ionic.

The pH of the ink is preferably from 4 to 10.

When the ink according to the third aspect of the invention is used as an ink jet printing ink, the ink preferably has a concentration of less than 100 parts per million, more preferably less than 50 parts per million, in total of halide ions and divalent and trivalent metals. This reduces nozzle blockage in ink jet printing heads, particularly in thermal ink jet printers. The inks may be purified using conventional techniques, for example ultrafiltrating reverse osmosis, dialysis or a combination thereof.

A fourth aspect of the present invention provides a process for printing an image on a substrate comprising applying thereto by means of an ink jet printer an ink containing a compound according to the first aspect of the invention or a composition according to the second aspect of the invention.

The ink used in this process is preferably as defined in the third aspect of the present invention The ink jet printer preferably applies the ink to the substrate in the form of droplets which are ejected through a small orifice onto the substrate. Preferred ink jet printers are piezoelectricink jet printers and thermal ink jet printers. In thermal ink jet printers, programmed pulses of heat are applied to the ink in a reservoir by means of a resistor adjacent to the orifice, thereby causing the ink to be ejected in the form of small droplets directed towards the substrate during relative movement between the substrate and the orifice. In piezoelectric inkjet printers the oscillation of a small crystal causes ejection of the ink from the orifice.

The substrate is preferably paper, plastic, a textile, metal or glass, more preferably paper, an overhead projector slide or a textile material, especially paper.

14 Preferred papers are plain or treated papers which may have an acid, alkaline or ( R7) neutral character. Examples of commercially available papers include, HP/ Premium ( RT") Coated Paper, HP/ Photopape,r (all available from Hewlett Packard Inc.), Stylus Pro 720 1 W-) (10-) dpi Coated Paper, Epson/'Photo Quality Glossy Film, Epson/Photo Quality Glossy Paper ( gTA) 01171- (available from Seiko Epson orp.), Canon/HR 101 High Resolution Paper, Canon/GP 201 Glossy Paper, CanonZ 101 High Gloss Film (all available from Canon Inc.), NH N ly-1) Wiggins Conqueror paper (available from Wiggins Teape Ltd), Xerox/Acid Paper and ( (271") L) XeroxAlkaline paper, XeroYAcid Paper (available from Xerox).

A fifth aspect of the present invention provides a substrate, preferably a paper, an overhead projector slide or a textile material, printed with an ink according to the third aspect of the present invention or by means of the process according to the fourth aspect of the present invention.

According to a sixth aspect of the present invention there is provided an ink jet printer cartridge comprising a chamber and ink, wherein the ink is present in the chamber and the ink contains a compound or a composition according to the second or third aspect of the invention. Preferably the ink is an ink according to the third aspect of the invention.

According to an eighth aspect of the present invention there is provided an ink jet printer containing an ink jet printer cartridge, wherein the ink jet printer cartridge is as defined in the seventh aspect of the present invention.

The invention is further illustrated by the following Examples in which all parts and percentages are by weight unless otherwise stated.

Example 1

Dye (11) S03H OH VN COOH HOOC-q N 111, N 1 N N N:- 0 H N -_ N HO 3 S -- H H H \ N OH N HO S03H WN N HOOCb H H03S Dye (1) Dye 1 was prepared in accordance with the following process:

Stage (a): Diazotisation and Coupling Anthranilic acid (13.7g, 0.1 M) was dissolved in 500mi water at pH 8 (2M NaOH), screened then added sodium nitrite (8.28g, 0. 1 2M). 30mi concentrated hydrochloric acid in 1 00mi ice and water at <50C was to this solution at <50C over 20 minutes. The mixture was then stirred for 2 hours at <50C and excess nitrous acid was destroyed using sulphamic acid.

Acetyl H-acid (51.8g, 0. 1 M) was dissolved in 500mi water, screened then allowed to stir at <50C while the above solution was added slowly over 30 minutes whilst maintaining the pH 7-8 with 2M NaOH and the temperature <50C. The mixture was left to stir for 2hours at <50C and pH 7-8, then the product was salted out using 20% w/v NaCI.

The precipitate was filtered off and washed well with saturated brine then pulled dry on a filter.

Stage (b): Hydrolysis The product of stage (a) was hydrolysed in 1 litre of water and 170mi concentrated is sodium hydroxide at 8WC for 4 hours. The solution was then neutralised while hot to pH 8 using concentrated hydrochloric acid. The product was salted out by addition of 20% w/v NaCI, filtered off and washed well with saturated brine, pulled dry on a filter and then dried in the oven at 500C.

Stage (c): Condensation with Cyanuric Chloride The product of stage (b) (11.7 parts) was stirred in water (400 parts) adjusted to pH 8.5 using 2M NaOH. The resulting suspension was cooled to <50C then a slurry of cyanuric chloride (5.1 parts) dispersed in water (25 parts) with calsolene oil(O.1 parts) was added and the reaction mixture was left to stir at <50C for 2 hours maintaining pH 6.5 by the addition of 2M NaOH.

Stne (d): Condensation with DL-Lysine DL-Lysine (2 parts) was then added to the reaction mixture in stage (c). The pH was raised to 8.5 with 2M sodium hydroxide and the temperature raised to 250C. Stirred at 250C/pH 8.5 for 3 hours.

Stage (e): Hydrolysis 1,4-diazabicyclo[2,2,2]octane (0.1 part) was added to the reaction mixture. The pH was raised to 11 with 2M sodium hydroxide and the temperature was raised to 800C.

Stirred at pH 111800C for 1 hour to complete the hydrolysis. Sodium chloride was added to 20% w/v and the pH reduced to 5 with concentrated hydrochloric acid. The mixture was cooled to 600C and the product filtered off and washed with 15% sodium chloride solution.

Stage (f): Purification The product of stage (e) was dissolveo in dilute sodium hydroxide solution and (fl -i) dialysed to low conductivity using Visking tubing. The dialysed solution was filtered 16 through Whatman/GIFF filter paper and the filtered solution evaporated to dryness to give the title product, 12 parts.

Example 2 to 4 so 3 H OH N N H L-N HO 3 S H N OH 0 H Nz:-N N HOOCO H N OH HOOC 1 NZ N)Z:ll HO 3 S S03 H Formula (A) Dyes of the Formula (A) were prepared by condensing the compound of the formula XHI-L-XlHI shown in Table 1 with approximately 2 molar equivalents of the product of stage (c) in Example 1. The resulting product was then hydrolysed by heating in aqueous sodium hydroxide to give the title product.

Table 1

Example XH-L-M 2 N1H2CH(COOH)CH2SSCH2CH(COOH)N1H12 3 N1H2CH(COOH)(CH2)31MH2 4 NH12CH(COOH)CH2SH ExamiDle 5 is Dye (51 so 3 H NH H N N COOH COOH Ll, s-S,. H N N N N H 0 3 S- H H N nO H N'\- N H HOOC ≥=:N HOOC H N 0 H N,, N H 0 3 S so 3H Dye (5) Dye(5) was prepared by condensing the diamine of the formula NH2CH(COOH)CH2-SS-CH2CH(COOH)NH2 with approximately 2 molar equivalents of the product of stage (c) in Example 1. The resulting product was then condensed with 2 molar equivalents of 2-(2-aminoethoxy) ethanol. The pH was raised to 9.7 using 2M NaOH, then the solution was heated at 900C whilst maintaining the pH at 9. 7 using 2M NaOH for 1 hour.

Example 6 to 9 S03H Z N N H L-N N N H" N H pe.,u N z H03S OH 5 N:;,N HN /--N OH HOOC HOOC '&CH3 H03S S03H CH3 Formula (B) Dyes of the Formula (B) were prepared using an analogous process to that described in Example 5 except that the anthranilic acid was replaced with 6-methyl is anthranilic acid; the 2-(2-aminoethoxy)ethanol was replaced with the compound of the formula ZH shown in Table 2; and in place of the diamine of the formula NH2CH(COOH)CH2-SS-CH2CH(COOH)NH2 there was used the diamine of the formula NH2LNH2 shown in Table 2.

Table 2

Example ZH XH-L-XH 6 2-(2-aminoethoxy)ethanol NH2CH(COOH)CH2SSCH2(COOH)NH2 7 2-aminoethylphosphonic acid NH2CH(COOH)CH2SSCH2CH(COOH)NH2 8 2,3-dihydroxypropylamine NH2CH(COOH)(CH2)3NH2 9 morpholine NH2CH(COOH)(CH2)3NH2 18 Examples 10 to 12 so 3 H OH N J"' N H / /N "9"' N L-N H 0 3 S-- H H OH N \- OH N \- N HOOC N, HN OH HOOC '&CH 3 S, N CH 3 H 0 3 so 3 H Formula (C) Dyes of the Formula (C) were prepared using an analogous process to that described in Example 1 except that the anthranilic acid was replaced with 6-methyl anthranilic acid; and in place of DL-Lysine there was used the diamine of the formula NH,Li\1H2 shown in Table 3.

Table 3

Example NH2LNH2 NH2CH(COOH)CH2SSCH2CH(COOH)N1H12 11 NH2CH(COOH)(CH2)3NH2 12 NIHI2CH(COOH)CH2SSCH2CH(COOH)NH2 Example 13: Inks and Ink Jet Prin "n The dyes described in Examples 1 to 13 were formulated into inks by dissolving 3.5 parts of the dye in 96.5 parts of a medium (adjusted to pH 9.5 with ammonium hydroxide) comprising:

parts 2-pyrrolidone; parts thiodiglycol.

2 parts Surfynol4465 (a non-ionic surfactant available from Air Products Inc.); and 88 parts water.

The resulting solution was then filtered through a 0.45gm filter.

When ink jet printed onto paper, the inks provided prints with a bright magenta shade, high water-fastness and good light fastness.

19 Liqht-Fastness Measurement The inks described above containing the dyes shown in Table 4 were printed onto ( 12A-) (("7)-) the substrates shown in Table 4 using a Hewlett Packard ADeskJet/690c inkjet printer.

After drying, each print was mounted, half covered, in an Atlas Ci35a weatherometer and irradiated for 100 hours. The prints were removed and the reflected optical density of the exposed and covered portions measured using an X- Rite TM938 densitometer. These readings were used to calculate the optical density loss following the irradiation (AE).

The light-fastness results for each substrate (AE) are shown in Table 4. A low figure for AE indicates low fading, i.e. high light-fastness.

Table 4

Dye Present in the Ink Substrate Light-fastness (AE) Example 5 HR 101 29 Example 5 HG 201 16 Example 5 GP 201 21 Example 2 HR 101 20 Example 2 HG 201 12 Example 2 GP 201 13 In Table 4 the following abbreviations are used:

HR 101 is Canon HR101 coated inkjet paper, ex Canon Inc.

HG 201 is Canon HG 201 glossy film, ex Canon Inc.

GP 201 is Canon GP 201 glossy paper, ex Canon Inc.

Example 14

The inks described in Table 5, 6 and 7 may be prepared wherein the Dye described in the first column is the Dye made in the above Examples 1 to 5 of the corresponding number. Numbers quoted in the second column onwards refer to the number of parts of the relevant ingredient and all parts are by weight. The inks may be applied to paper by thermal or piezo ink jet printing.

The following abbreviations are used in Tables 5 to 7:

2S PG = propylene glycol DEG = diethylene glycol NMP N-methyl pyrrolidone TIFP = 2,2,3,3-tetrafluoropropanol CYC cyclohexanol 2P = 2-pyrrolidone P12 = propane- 1,2-diol UR = Urea CET= cetyl ammonium bromide PHO = Na2HPO, and TBT = tertiary butanol TDG = thiodiglycol GLY = glycerol P-1,5 = Pentane-1,5-diol H - 1,6 = Hexane 1,6-diol CAP = caprolactone CAP-L = caprolactam TEA = triethanolamine EG = ethylene glycol BUT = y-butyrolactone DEG-MBE = diethylene glycol monobutyl ether PEG 200 = Polyethylene glycol (average molecular weight of 200) TABLE 5

Ink Dye Dye Water PG DEG NMP P-1,5 TEA CYC BUT CAP EG CAP-L Content 1 1 3.0 90 5 4.8 0.2 2 2 10.0 85 3 3 3 5 3 2 2.1 91 8 1 1 4 3 3.1 86 5 0.2 4 4.8 4 1.1 81 9 0.5 0.5 6 5 2.5 60 4 15 3 3 6 9 4 7 4 5 65 20 5 10 5 8 3 2.4 75 5 4 5 6 5 9 3 4.1 80 3 5 2 9.7 0.3 1 3.2 65 5 4 6 5 4 5 11 1 5.1 96 4 6 12 5 10.8 90 5 5 13 5 10.0 80 2 6 2 5 1 14 3 1.8 80 5 4 5 2.6 84 11 15 16 5 3.3 80 2 10 2 5 6 17 5 12.0 90 7 0.3 2.7 18 2 5.4 69 2 20 2 1 3 3 N) -X TABLE 6

Ink Dye Dye Water GLY DEG NMP CET TBT TDG UR PHO 2P P12 Content 19 1 3.0 80 15 0.2 4.8 2 9.0 90 5 1.2 5 21 3 1.5 85 3.8 5 0.16 4.64 0.2 22 4 2.5 90 6 3.88 0.12 23 5 3.1 82 4 8 0.3 5.7 24 3 0.9 85 10 4.8 0,2 2 8.0 90 4.7 5 0.3 26 1 4.0 70 10 4 1 4 11 27 2 2.2 75 4 10 3 2 6 28 1 10,0 91 6 3 29 5 9.0 76 9 7 2.05 0.95 5 3 5.0 78 5 11 6 31 1 5.4 86 7 7 32 1 2.1 70 5 5 5 0.1 0.2 0.1 5 0.1 9.5 33 3 2.0 90 10 34 2 2 88 2 10 4 5 78 5 12 5 36 2 8 70 2 8 15 5 37 1 10 80 8 12 38 4 10 80 10 r\j N) TABLE 7

Ink Dye Dye Water PEG DEG- NMP H-1,6 TEA TFP BUT CAP EG CAP-L Content 200 MBE 39 1 2.0 80 5 6 4 5 2 3.0 90 5 4.8 0.2 41 3 10.0 85 3 3 3 5 1 42 4 2.1 91 8 1 43 5 3.1 86 5 0.2 3.8 5 44 3 1.1 81 9 0.5 0.5 9 1 2.5 60 4 15 3 3 6 5 4 46 3 5 65 20 10 47 5 2.4 75 5 4 5 6 5 48 5 4.1 80 3 5 2 9.7 0.3 49 1 3.2 70 5 4 6 5 4 6 5 1 5.1 96 4 51 1 10.8 90 5 5 52 2 10.0 80 2 6 2 5 1 4 53 3 1.8 80 5 15 54 4 2.6 84 11 5 5 3.3 80 2 10 2 6 56 4 12.0 90 7 0.3 2.8 57 2 5.4 69 2 20 2 1 3 3 58 2 6.0 91 4 5 Ni W 24

Claims

CLAIMS A compound of the Formula (1) and salts thereof:

1 N1' N N z N R \ 1, ".5 1 R OH N A X-L- A'-N- OurH Ar-INI=N N=N-Ar 1 HO P 3 so 3 H 3H so 3 H Formula (1) wherein:

each A independently is N, C-Cl, C-CN or C-N02; each Ar independently is a substituted aryl group carrying a -COOH group ortho to the azo (N=N-) group; L is an aliphatic group carrying a -COOH, -S03H or -P03H2group; each Z independently is -SR 2, -OR 3, -NR 4 R 5 or a labile atom or group; is each X independently is -S-, -0- or -NW-; each R' independently is H or optionally substituted alkyl; and R 2, R 3, R' and R' are independently H, optionally substituted alkyl, optionally substituted aryl or optionally substituted aralkyl; or R' and R' together with the nitrogen to which they are attached form an optionally substituted five or six membered ring.

2. A compound according to claim 1 wherein each Ar independently is optionally substituted 1 -carboxy-naphth2-yi or optionally substituted 2carboxy phenyl.

3. A compound according to either claim 1 or claim 2 wherein each Ar is 2carboxyphenyl.

4. A compound according to any one of the preceding claims wherein each Z independently is -SR 2, -OR' or -NR 4 R5 wherein R 2 R 3, R 4 and R' are as defined in claim 1. 30

5. A compound according to any one of the preceding claims wherein L is an optionally interrupted alkenylene group or an optionally interrupted alkylene group containing up to 20 carbon atoms, said group carrying a substituent selected from -COOH, -S03H and -P03H2.

6. A compound according to any one of the preceding claims wherein L is an optionally interrupted C2-20-alkylene group which carries a substituent selected from _S03H, -COOH and -P03H2.

7. A compound according to either claim 6 or claim 7 wherein L is optionally interrupted by one or more of -0-, -S-, -SS- or NR' wherein R' is as defined in claim 1.

8. A compound according to claim 1 of the Formula (4) and salts thereof:

Z1 Z1 N'-N N"N COOH R 11 R 11 COOH N OH OH N'J"N;NR" L' NR1 Ni -N" N-1 NN - N HO 3 S S03 H H03S"' SO3H Formula (4) wherein:

L' is aC2-2,-alkylene group carrying a-S03H or -COOH group; each W' independently is H or Cl,-alkyl optionally substituted by OH, - COOH, _S03H or -CN; each Z1 independently is -SR 2, -OR 3 or -NR 4 R'; and R 2, R 3, R' and R' are as defined in claim 1.

9. A compound according to claim 8 wherein each Z1 independently is -OH, SH or -NR'R", wherein R' and R10 each independently is H, Cl_.-aikyl optionally substituted by -OH, Cl-4-alkoxy, Cl-4-hydroxyalkoxy, -COOH or -S03H.

10. A composition comprising:

(a) one or more compound according to any one of the preceding claims; and (b) one or more water-soluble magenta dye other than a compound according to any one of the preceding claims.

11. An ink comprising: (a) a compound according to any one of claims 1 to 9, or a composition according to claim 10; and (b) a liquid medium.

26

12. A process for printing an image on a substrate comprising applying thereto by means of an ink jet printer an ink containing a compound according to any one of claims 1 to 9 or a composition according to claim 10.

13. A substrate printed with an ink according to claim 11 or by means of the process according to claim 12.

14. An ink jet printer cartridge comprising a chamber and ink, wherein the ink is present in the chamber and the ink contains a compound according to any one of claims 1 to 9 or a composition according to claim 10.

15. An ink jet printer containing an ink jet printer cartridge, wherein the ink jet printer cartridge is as defined in claim 14. is

16. A dye substantially as herein described with reference to any one of the examples.

17. An ink substantially as herein described with reference to any one of the examples.