AU7410400A - Composition and method for bleaching a substrate - Google Patents

Description

WO 01/16271 PCT/EPOO/08076 COMPOSITION AND METHOD FOR BLEACHING A SUBSTRATE FIELD OF INVENTION 5 This invention relates to compositions and methods for catalytically bleaching substrates with atmospheric oxygen, using a metal-ligand complex as catalyst, which compositions are formulated as liquids. This invention also relates to a method of treating textiles, such as laundry fabrics, using 10 a metal-ligand complex as catalyst whereby bleaching with atmospheric oxygen is catalysed after the treatment, wherein the treatment composition is formulated as a liquid. BACKGROUND OF INVENTION 15 Peroxygen bleaches are well known for their ability to remove stains from substrates. Traditionally, the substrate is subjected to hydrogen peroxide, or to substances which can generate hydroperoxyl radicals, such as inorganic or 20 organic peroxides. Generally, these systems must be activated. One method of activation is to employ wash temperatures of 60 0 C or higher. However, these high temperatures often lead to inefficient cleaning, and can also cause premature damage to the substrate. 25 A preferred approach to generating hydroperoxyl bleach species is the use of inorganic peroxides coupled with organic precursor compounds. These systems are employed for many commercial laundry powders. For example, various 30 European systems are based on tetraacetyl ethylenediamine (TAED) as the organic precursor coupled with sodium WO 01/16271 PCT/EPOO/08076 -2 perborate or sodium percarbonate, whereas in the United States laundry bleach products are typically based on sodium nonanoyloxybenzenesulphonate (SNOBS) as the organic precursor coupled with sodium perborate. 5 Precursor systems are generally effective but still exhibit several disadvantages. For example, organic precursors are moderately sophisticated molecules requiring multi-step manufacturing processes resulting in high capital costs. 10 Also, precursor systems have large formulation space requirements so that a significant proportion of a laundry powder must be devoted to the bleach components, leaving less room for other active ingredients and complicating the development of concentrated powders. Moreover, precursor 15 systems do not bleach very efficiently in countries where consumers have wash habits entailing low dosage, short wash times, cold temperatures and low wash liquor to substrate ratios. 20 Alternatively, or additionally, hydrogen peroxide and peroxy systems can be activated by bleach catalysts, such as by complexes of iron and the ligand N4Py (i.e. N, N bis(pyridin-2-yl-methyl)-bis(pyridin-2-yl)methylamine) disclosed in W095/34628, or the ligand Tpen (i.e. N, N, N', 25 N'-tetra(pyridin-2-yl-methyl)ethylenediamine) disclosed in W097/48787. These publications do not foresee a role in providing storage stable liquid bleaching compositions even if, according to these publications, molecular oxygen may be used as the oxidant as an alternative to peroxide generating 30 systems.

WO 01/16271 PCT/EPOO/08076 -3 As discussed by N.J. Milne in J. of Surfactants and Detergents, Vol 1, no 2, 253-261 (1998), it has long been thought desirable to be able to use atmospheric oxygen (air) as the source for a bleaching species. The use of 5 atmospheric oxygen (air) as the source for a bleaching species would avoid the need for costly hydroperoxyl generating systems. Unfortunately, air as such is kinetically inert towards bleaching substrates and exhibits no bleaching ability. Recently some progress has been made 10 in this area. For example, WO 97/38074 reports the use of air for oxidising stains on fabrics by bubbling air through an aqueous solution containing an aldehyde and a radical initiator. A broad range of aliphatic, aromatic and heterocyclic aldehydes is reported to be useful, 15 particularly para-substituted aldehydes such as 4-methyl-, 4-ethyl- and 4-isopropyl benzaldehyde, whereas the range of initiators disclosed includes N-hydroxysuccinimide, various peroxides and transition metal coordination complexes. 20 However, although this system employs molecular oxygen from the air, the aldehyde component and radical initiators such as peroxides are consumed during the bleaching process. These components must therefore be included in the composition in relatively high amounts so as not to become 25 depleted before completion of the bleaching process in the wash cycle. Moreover, the spent components represent a waste of resources as they can no longer participate in the bleaching process. 30 Accordingly, it would be desirable to be able to provide a bleaching system based on atmospheric oxygen or air that WO 01/16271 PCT/EPOO/08076 -4 does not rely primarily on hydrogen peroxide or a hydroperoxyl generating system, and that does not require the presence of organic components such as aldehydes that are consumed in the process. Moreover, it would be 5 desirable to provide such a bleaching system that is effective in aqueous medium. It may also be noted that the known art teaches a bleaching effect only as long as the substrate is being subjected to 10 the bleaching treatment. Thus, there is no expectation that hydrogen peroxide or peroxy bleach systems could continue to provide a bleaching effect on a treated substrate, such as a laundry fabric after washing and drying, since the bleaching species themselves or any activators necessary for the 15 bleaching systems would be assumed to be removed from the substrate, or consumed or deactivated, on completing the wash cycle and drying. It would be therefore also be desirable to be able to treat 20 a textile such that, after the treatment is completed, a bleaching effect is observed on the textile. Furthermore, it would be desirable to be able to provide a bleach treatment for textiles such as laundry fabrics whereby residual bleaching occurs in the presence of air when the 25 treated fabric has been treated and is dry. It would be desirable for the residual bleaching of dry textiles to be conducted irrespective of exposure to light. A further disadvantage associated with conventional 30 bleaching compositions based on hydrogen peroxide or peroxy systems such those containing organic peroxyacids is that WO 01/16271 PCT/EPOO/08076 -5 the compositions tend to be chemically or physically unstable in the presence of liquid solvents, carriers or other liquid components such as surfactants, particularly when formulated as aqueous compositions. Consequently, when 5 formulated as liquids, these bleaching compositions on the one hand do not exhibit satisfactory storage stability, resulting in a rapid loss of bleaching activity or in a loss of structural integrity, for example phase separation, or require the incorporation of additional stabilising systems 10 to minimise these effects with attendant disadvantages in terms of cost or processing. Decomposition of a hydrogen peroxide or peroxy liquid bleaching composition in a sealed container leads to an increase in the internal pressure of the sealed container. The increase in the internal 15 pressure leads to the possibility of the sealed container rupturing in a dangerous manner. In the presence of surfactants, decomposition of the hydrogen peroxide or peroxy liquid bleaching composition leads to foaming of the composition. On the other hand, liquid bleaching 20 compositions are conveniently dosed into containers for storage or for use, or otherwise handled, and are desired by the consumer, particularly in the United States of America. It would therefore also be desirable to be able to provide a 25 bleaching composition in the form of a liquid, which is chemically and physically stable, without at least some of the disadvantages hitherto associated with liquid bleaching compositions. It would furthermore be desirable to be able to provide chemically and physically storage stable 30 detergent bleaching compositions or rinse conditioning bleach compositions in the form of a liquid.

WO 01/16271 PCT/EPOO/08076 -6 Application WO00/29537, filed 9 November 1999, was published after the filing date of the present application disclosing theoretical examples of compositions for bleaching with a transition metal complex in the absence of an added 5 peroxygen bleach. Application WO00/29537 has no evidence of efficacy and includes two classes of ligands: some cross bridged macrocyclic ligands and some macrocyclic ligands. The macrocyclic ligands are disclosed as manganese complexes and are not found in the priority document of WOOO/29537; 10 namely US serial number 60/108,292 filed 13 November 1998. The theoretical examples given are for a heavy-duty granular laundry detergent and heavy-duty liquid laundry detergent. In both these examples the exemplified bleach catalyst is 5,12-dimethyl-1,5,8,12-tetra-bicyclo[6.6.2.]hexadecane 15 manganese (II) chloride. There are no examples demonstrating any bleaching effect. The use of manganese complexes in laundry applications is less preferred because of dye/textile damage under specific conditions. 20 SUMMARY OF INVENTION We have now found that it is possible to achieve a chemically and physically stable bleaching composition in the form of a liquid, by using an organic substance that 25 forms a complex which catalyses the bleaching of substrates using atmospheric oxygen or air, and formulating the organic substance in a liquid that is substantially devoid of peroxygen bleach or a peroxy-based or -generating bleach system. Moreover, we have found that these organic 30 substances can be formulated together with detergent or rinse conditioning agents, in a liquid that is substantially WO 01/16271 PCT/EPOO/08076 -7 devoid of peroxygen bleach or a peroxy-based or -generating bleach system, to provide chemically and physically stable detergent bleaching compositions or rinse conditioning bleach compositions, in the form of a liquid. 5 Accordingly, in a first aspect, the present invention a liquid bleaching composition comprising an organic substance which forms a complex with a transition metal, the complex catalysing bleaching of a substrate by atmospheric oxygen, 10 and a liquid carrier or solvent, wherein the composition is substantially devoid of peroxygen bleach or a peroxy-based or -generating bleach system. The composition is therefore preferably insensitive or stable to catalase, which acts on peroxy species. 15 In a second aspect, the present invention provides a method of bleaching a substrate comprising applying to the substrate a liquid bleaching composition that comprises an organic substance which forms a complex with a transition 20 metal, the complex catalysing bleaching of the substrate by atmospheric oxygen, and a liquid carrier or solvent, wherein the composition is substantially devoid of peroxygen bleach or a peroxy-based or -generating bleach system. 25 Furthermore, in a third aspect, the present invention provides the use of an organic substance which forms a complex with a transition metal, the complex catalysing bleaching of a substrate by the atmospheric oxygen, as a catalytic bleaching agent in a liquid bleaching composition 30 substantially devoid of peroxygen bleach or a peroxy-based or -generating bleach system.

WO 01/16271 PCT/EPOO/08076 -8 We have also found that the liquid bleaching compositions in accordance with the present invention are surprisingly effective in catalysing bleaching of substrates by atmospheric oxygen after treatment of the substrate. 5 Accordingly, in a fourth aspect, the present invention provides a method of treating a textile by contacting the textile with a liquid bleaching composition that comprises an organic substance which forms a complex with a transition 10 metal, the complex catalysing bleaching by atmospheric oxygen, and a liquid carrier or solvent, wherein the composition is substantially devoid of peroxygen bleach or a peroxy-based or -generating bleach system, whereby the complex catalyses bleaching of the textile by atmospheric 15 oxygen after the treatment. The present invention requires all or the majority of the bleaching species in the liquid bleaching composition (on an equivalent weight basis) to be derived from atmospheric 20 oxygen. Thus, the liquid composition will be made wholly or substantially devoid of peroxygen bleach or a peroxy-based or -generating bleach system. The organic substance is a catalyst for the bleaching process and, as such, is not consumed but can continue to participate in the bleaching 25 process. Since the bleaching system of the type used in the liquid bleaching composition is catalytically activated and the bleaching species is derived from atmospheric oxygen, the present invention is advantageous in that it provides a bleaching composition which is not only convenient to handle 30 by virtue of being in the form of a liquid, but which also is both cost-effective and environmentally friendly.

WO 01/16271 PCT/EPOO/08076 -9 The liquid bleaching composition may be formulated as a concentrated bleaching liquid for direct application to a substrate, or for application to a substrate following dilution, such as dilution before or during use of the 5 liquid composition by the consumer or in washing apparatus. The liquid bleaching composition can for example be formulated as an aqueous medium, or so as to be dispersable into an aqueous medium, and is therefore particularly 10 applicable to bleaching of laundry fabrics. Therefore, whilst the composition and method according to the present invention may be used for bleaching any suitable substrate, the preferred substrate is a laundry fabric. Bleaching may be carried out by simply leaving the substrate in contact 15 for a sufficient period of time with a bleach medium constituted by or prepared from the liquid bleaching composition. Preferably, however, the bleach medium on or containing the substrate is agitated. 20 An advantage of the method according to the fourth aspect of the invention is that, by enabling a bleaching effect even after the textile has been treated, the benefits of bleaching can be prolonged on the textile. Furthermore, since a bleaching effect is conferred to the.textile after 25 the treatment, the treatment itself, such as a laundry wash cycle, may for example be shortened. The present invention also extends to a commercial package comprising a liquid bleaching composition comprising a 30 ligand or complex as defined below together with instructions for its use.

WO 01/16271 PCT/EPOO/08076 - 10 The present invention also extends to use of a ligand or complex as defined below in the manufacture of a liquid bleaching composition, the bleaching composition substantially devoid of peroxygen bleach or a peroxy-based 5 or peroxy-generating bleach system. DETAILED DESCRIPTION OF THE INVENTION The catalyst may comprise a preformed complex of a ligand 10 and a transition metal. Alternatively, the catalyst may comprise a free ligand that complexes with a transition metal already present in the water or that complexes with a transition metal present in the substrate. The catalyst may also be included in the form of a composition of a free 15 ligand or a transition metal-substitutable metal-ligand complex, and a source of transition metal, whereby the complex is formed in situ in the medium. It is preferred that the catalyst is a pentadentate ligand or complex thereof. 20 The ligand forms a complex with one or more transition metals, in the latter case for example as a dinuclear complex. Suitable transition metals include for example: manganese in oxidation states II-V, iron II-V, copper I-III, 25 cobalt I-III, titanium II-IV, tungsten IV-VI, vanadium II-V and molybdenum II-VI. The transition metal complex preferably is of the general formula: 30 [MaLkXn] Ym WO 01/16271 PCT/EPOO/08076 - 11 in which: M represents a metal selected from Mn(II)-(III)-(IV) (V), Cu(I)-(II)-(III), Fe (II)-(III)-(IV)-(V), Co(I)-(II) 5 (III), Ti(II)-(III)-(IV), V(II)-(III)-(IV)-(V), MO(II) (III)-(IV)-(V)-(VI) and W(IV)-(V)-(VI), preferably from Fe(II)-(III)-(IV)-(V); L represents the ligand, preferably N,N-bis(pyridin-2 yl-methyl)-1,1-bis(pyridin-2-yl)-1-aminoethane, or its 10 protonated or deprotonated analogue; X represents a coordinating species selected from any mono, bi or tri charged anions and any neutral molecules able to coordinate the metal in a mono, bi or tridentate manner; 15 Y represents any non-coordinated counter ion; a represents an integer from 1 to 10; k represents an integer from 1 to 10; n represents zero or an integer from 1 to 10; m represents zero or an integer from 1 to 20. 20 Preferably, the complex is an iron complex comprising the ligand N,N-bis(pyridin-2-yl-methyl)-1,1-bis(pyridin-2-yl)-1 aminoethane. However, it will be appreciated that the pretreatment method of the present invention may instead, or 25 additionally, use other ligands and transition metal complexes, provided that the complex formed is capable of catalysing stain bleaching by atmospheric oxygen. Suitable classes of ligands are described below: 30 (A) Ligands of the general formula (IA): WO 01/16271 PCT/EPOO/08076 - 12 Z1-(Q1)\ T C-(Q3)--U Z1-(Q1) (IA) wherein 5 Zi groups independently represent a coordinating group selected from hydroxy, amino, -NHR or -N(R) 2 (wherein R=Ci-G alkyl), carboxylate, amido, -NH-C(NH)NH 2 , hydroxyphenyl, a heterocyclic ring optionally substituted by one or more functional groups E or a heteroaromatic ring optionally 10 substituted by one or more functional groups E, the heteroaromatic ring being selected from pyridine, pyrimidine, pyrazine, pyrazole, imidazole, benzimidazole, quinoline, quinoxaline, triazole, isoquinoline, carbazole, indole, isoindole, oxazole and thiazole; 15 Q1 and Q3 independently represent a group of the formula: 5 P7 R6 R8 20 wherein WO 01/16271 PCT/EPOO/08076 - 13 5 > a+b+c > 1; a=0-5; b=0-5; c=0-5; n=O or 1 (preferably n=0); Y independently represents a group selected from -0-, 5 S-, -SO-, -SO 2 -, -C(0)-, arylene, alkylene, heteroarylene, heterocycloalkylene, -(G)P-, -P(O)- and -(G)N- , wherein G is selected from hydrogen, alkyl, aryl, arylalkyl, cycloalkyl, each except hydrogen being optionally substituted by one or more functional groups E; 10 R5, R6, R7, R8 independently represent a group selected from hydrogen, hydroxyl, halogen, -R and -OR, wherein R represents alkyl, alkenyl, cycloalkyl, heterocycloalkyl, aryl, heteroaryl or a carbonyl derivative group, R being 15 optionally substituted by one or more functional groups E, or R5 together with R6, or R7 together with R8, or both, represent oxygen, or R5 together with R7 and/or independently R6 together with R8, or R5 together with R8 and/or independently R6 20 together with R7, represent Cia-alkylene optionally substituted by Ci 4 -alkyl, -F, -Cl, -Br or -I; T represents a non-coordinated group selected from hydrogen, hydroxyl, halogen, -R and -OR, wherein R represents alkyl, alkenyl, cycloalkyl, heterocycloalkyl, 25 aryl, arylalkyl, heteroaryl or a carbonyl derivative group, R being optionally substituted by one or more functional groups E (preferably T= -H, -OH, methyl, methoxy or benzyl); U represents either a non-coordinated group T 30 independently defined as above or a coordinating group of the general formula (IIA), (IIIA) or (IVA): WO 01/16271 PCT/EPOO/08076 - 14 / (Q2)- Z2 -N (Q)-Z4 (IIA) (IIIA) (Q1)-Z1 -- Q -(Q3)-T (Q)-Zi (IVA) 10 wherein Q2 and Q4 are independently defined as for Q1 and Q3; 15 Q represents -N(T)- (wherein T is independently defined as above), or an optionally substituted heterocyclic ring or an optionally substituted heteroaromatic ring selected from pyridine, pyrimidine, pyrazine, pyrazole, imidazole, benzimidazole, quinoline, quinoxaline, triazole, 20 isoquinoline, carbazole, indole, isoindole, oxazole and thiazole; Z2 is independently defined as for Zi; WO 01/16271 PCT/EPOO/08076 - 15 Z3 groups independently represent -N(T)- (wherein T is independently defined as above); Z4 represents a coordinating or non-coordinating group 5 selected from hydrogen, hydroxyl, halogen, -NH-C(NH)NH 2 , -R and -OR, wherein R= alkyl, alkenyl, cycloalkyl, heterocycloalkyl, aryl, heteroaryl or a carbonyl derivative group, R being optionally substituted by one or more functional groups E, or Z4 represents a group of the general 10 formula (IIAa): Z2----( ) /(Ql)-Zl N (Q3) T / (Q1)-Z1 (IIAa) and 15 1 < j < 4. Preferably, Z1, Z2 and Z4 independently represent an optionally substituted heterocyclic ring or an optionally substituted heteroaromatic ring selected from pyridine, 20 pyrimidine, pyrazine, pyrazole, imidazole, benzimidazole, quinoline, quinoxaline, triazole, isoquinoline, carbazole, indole, isoindole, oxazole and thiazole. More preferably, Z1, Z2 and Z4 independently represent groups selected from optionally substituted pyridin-2-yl, optionally substituted 25 imidazol-2-yl, optionally substituted imidazol-4-yl, optionally substituted pyrazol-1-yl, and optionally substituted quinolin-2-yl. Most preferred is that Z1, Z2 and Z4 each represent optionally substituted pyridin-2-yl.

WO 01/16271 PCT/EPOO/08076 - 16 The groups Z1, Z2 and Z4 if substituted, are preferably substituted by a group selected from C 1 4 -alkyl, aryl, arylalkyl, heteroaryl, methoxy, hydroxy, nitro, amino, carboxyl, halo, and carbonyl. Preferred is that Z1, Z2 and 5 Z4 are each substituted by a methyl group. Also, we prefer that the Z1 groups represent identical groups. Each Q1 preferably represents a covalent bond or Cl-C4 alkylene, more preferably a covalent bond, methylene or 10 ethylene, most preferably a covalent bond. Group Q preferably represents a covalent bond or Cl-C4 alkylene, more preferably a covalent bond. 15 The groups R5, R6, R7, R8 preferably independently represent a group selected from -H, hydroxy-Co-C 20 -alkyl, halo-Co-C 20 alkyl, nitroso, formyl-Co-C 20 -alkyl, carboxyl-Co-C 20 -alkyl and esters and salts thereof, carbamoyl-Co-C 20 -alkyl, sulfo-Co

C

20 -alkyl and esters and salts thereof, sulfamoyl-Co-C 20 20 alkyl, amino-Co-C 20 -alkyl, aryl-Co-C 20 -alkyl, Co-C 20 -alkyl, alkoxy-Co-C 8 -alkyl, carbonyl-Co-C 6 -alkoxy, and Co-C 2 0 alkylamide. Preferably, none of R5-R8 is linked together. Non-coordinated group T preferably represents hydrogen, 25 hydroxy, methyl, ethyl, benzyl, or methoxy. In one aspect, the group U in formula (IA) represents a coordinating group of the general formula (IIA): WO 01/16271 PCT/EP00/08076 - 17 ,/ Q2-Z2 -N (Q#--z4 (IIA) According to this aspect, it is preferred that Z2 represents 5 an optionally substituted heterocyclic ring or an optionally substituted heteroaromatic ring selected from pyridine, pyrimidine, pyrazine, pyrazole, imidazole, benzimidazole, quinoline, quinoxaline, triazole, isoquinoline, carbazole, indole, isoindole, oxazole and thiazole, more preferably 10 optionally substituted pyridin-2-yl or optionally substituted benzimidazol-2-yl. It is also preferred, in this aspect, that Z4 represents an optionally substituted heterocyclic ring or an optionally 15 substituted heteroaromatic ring selected from pyridine, pyrimidine, pyrazine, pyrazole, imidazole, benzimidazole, quinoline, quinoxaline, triazole, isoquinoline, carbazole, indole, isoindole, oxazole and thiazole, more preferably optionally substituted pyridin-2-yl, or an non-coordinating 20 group selected from hydrogen, hydroxy, alkoxy, alkyl, alkenyl, cycloalkyl, aryl, or benzyl. In preferred embodiments of this aspect, the ligand is selected from: 25 1,1-bis(pyridin-2-yl)-N-methyl-N-(pyridin-2 ylmethyl)methylamine; 1,1-bis(pyridin-2-yl)-N,N-bis(6-methyl-pyridin-2 ylmethyl)methylamine; WO 01/16271 PCT/EPOO/08076 - 18 1, 1-bis (pyridin-2-yl) -N,N-bis (5-carboxymethyl-pyridin-2 ylmethyl)methylamine; 1,1-bis(pyridin-2-yl)-1-benzyl-N,N-bis(pyridin-2 ylmethyl)methylamine; and 5 1,1-bis(pyridin-2yl)-N,N-bis(benzimidazol-2 ylmethyl)methylamine. In a variant of this aspect, the group Z4 in formula (IIA) represents a group of the general formula (IIAa): 10 Z2---( ) /(Ql)~Zl N - (Q3)- C T (Q)-Zl (IIAa) In this variant, Q4 preferably represents optionally 15 substituted alkylene, preferably -CH 2

-CHOH-CH

2 - or -CH 2

-CH

2 CH 2 -. In a preferred embodiment of this variant, the ligand 1: Py Py Py P H-C-N N-C-H Py Py 20 wherein -Py represents pyridin-2-yl. In another aspect, the group U in formula (IA) represents a coordinating group of the general formula (IIIA): 25 WO 01/16271 PCT/EPOO/08076 - 19 Q 1 23 [L-2 Z3] (IIIA) wherein j is 1 or 2, preferably 1. 5 According to this aspect, each Q2 preferably represents (CH 2 )n- (n=2-4), and each Z3 preferably represents -N(R) wherein R = -H or C 1

.

4 -alkyl, preferably methyl. 10 In preferred embodiments of this aspect, the ligand is selected from: Py\ Me PY -Me H-C-N N Me-C-N N Py Py N N Me Me wherein -Py represents pyridin-2-yl. 15 In yet another aspect, the group U in formula (IA) represents a coordinating group of the general formula (IVA): Q1)-Z1 -Q - (Q3)- -T 20 (Q1)-Z1

(IVA)

WO 01/16271 PCT/EPOO/08076 - 20 In this aspect, Q preferably represents -N(T)- (wherein T= H, methyl, or benzyl) or pyridin-diyl. In preferred embodiments of this aspect, the ligand is 5 selected from: Py H Py Py Py Me-C-N-C-Me MeO-C-Q -C-OMe py Py Py Py Py Py HO-C-Q -- C--OH Py Py wherein -Py represents pyridin-2-yl, and -Q- represents 10 pyridin-2,6-diyl. (B) Ligands of the general formula (IB): R1-QQ R2--Q2 Q3"

R

3 15 (IB) wherein 20 n = 1 or 2, whereby if n = 2, then each -Q 3

-R

3 group is independently defined; WO 01/16271 PCT/EP00/08076 - 21 R 1 , R 2 , R 3 , R 4 independently represent a group selected from hydrogen, hydroxyl, halogen, -NH-C(NH)NH 2 , -R and -OR, wherein R= alkyl, alkenyl, cycloalkyl, heterocycloalkyl, aryl, heteroaryl or a carbonyl derivative group, R being 5 optionally substituted by one or more functional groups E, Qi, Q2, Q3, Q4 and Q independently represent a group of the formula: 5 P7 10 R6 R8 wherein 5 > a+b+c > 1; a=0-5; b=0-5; c=0-5; n=1 or 2; 15 Y independently represents a group selected from -0-, S-, -SO-, -SO 2 -, -C(O)-, arylene, alkylene, heteroarylene, heterocycloalkylene, -(G)P-, -P(O)- and -(G)N- , wherein G is selected from hydrogen, alkyl, aryl, arylalkyl, cycloalkyl, each except hydrogen being optionally 20 substituted by one or more functional groups E; R5, R6, R7, R8 independently represent a group selected from hydrogen, hydroxyl, halogen, -R and -OR, wherein R represents alkyl, alkenyl, cycloalkyl, heterocycloalkyl, WO 01/16271 PCT/EPOO/08076 - 22 aryl, heteroaryl or a carbonyl derivative group, R being optionally substituted by one or more functional groups E, or R5 together with R6, or R7 together with R8, or both, represent oxygen, 5 or R5 together with R7 and/or independently R6 together with R8, or R5 together with R8 and/or independently R6 together with R7, represent C 1

.

6 -alkylene optionally substituted by C 1

-

4 -alkyl, -F, -Cl, -Br or -I, 10 provided that at least two of R 1 , R 2 , R 3 , R 4 comprise coordinating heteroatoms and no more than six heteroatoms are coordinated to the same transition metal atom. At least two, and preferably at least three, of R 1 , R 2 , R 3 , R 4 15 independently represent a group selected from carboxylate, amido, -NH-C(NH)NH 2 , hydroxyphenyl, an optionally substituted heterocyclic ring or an optionally substituted heteroaromatic ring selected from pyridine, pyrimidine, pyrazine, pyrazole, imidazole, benzimidazole, quinoline, 20 quinoxaline, triazole, isoquinoline, carbazole, indole, isoindole, oxazole and thiazole. Preferably, substituents for groups R 1 , R 2 , R 3 , R 4 , when representing a heterocyclic or heteroaromatic ring, are selected from C 1

_

4 -alkyl, aryl, arylalkyl, heteroaryl, 25 methoxy, hydroxy, nitro, amino, carboxyl, halo, and carbonyl. The groups Q1, Q2, Q3, Q4 preferably independently represent a group selected from -CH 2 - and -CH 2

CH

2 -. 30 WO 01/16271 PCTEPOO/08076 - 23 Group Q is preferably a group selected from -(CH 2

)

2

-

4 -, CH 2 CH (OH) CH 2 -, optionally substituted by methyl or ethyl, OH N an , and 5 wherein R represents -H or C 1

-

4 -alkyl. Preferably, Qi, Q2, Q3, Q4 are defined such that a=b=0, c=1 and n=1, and Q is defined such that a=b=0, c=2 and n=1. 10 The groups R5, R6, R7, R8 preferably independently represent a group selected from -H, hydroxy-Co-C 20 -alkyl, halo-Co-C 2 0 alkyl, nitroso, formyl-Co-C 20 -alkyl, carboxyl-Co-C 20 -alkyl and esters and salts thereof, carbamoyl-Co-C 20 -alkyl, sulfo-Co

C

20 -alkyl and esters and salts thereof, sulfamoyl-C-C 20 15 alkyl, amino-Co-C 20 -alkyl, aryl-Co-C 20 -alkyl, Co-C 20 -alkyl, alkoxy-Co-Ce-alkyl, carbonyl-Co-C 6 -alkoxy, and Co-C 2 0 alkylamide. Preferably, none of RS-R8 is linked together. In a preferred aspect, the ligand is of the general formula 20 (IIB): RjQ\N-Q-N' 4R R2-Q2

Q

3

-R

3 (IIB) 25 wherein WO 01/16271 PCT/EPOO/08076 - 24 Q 1 , Q2, Q3, Q 4 are defined such that a=b=0, c=1 or 2 and n=1; Q is defined such that a=b=O, c=2,3 or 4 and n=1; and

R

1 , R 2 , R 3 , R 4 , R7, R8 are independently defined as for 5 formula (I). Preferred classes of ligands according to this aspect, as represented by formula (IIB) above, are as follows: 10 (i) ligands of the general formula (IIB) wherein:

R

1 , R 2 , R 3 , R 4 each independently represent a coordinating group selected from carboxylate, amido, -NH

C(NH)NH

2 , hydroxyphenyl, an optionally substituted heterocyclic ring or an optionally substituted 15 heteroaromatic ring selected from pyridine, pyrimidine, pyrazine, pyrazole, imidazole, benzimidazole, quinoline, quinoxaline, triazole, isoquinoline, carbazole, indole, isoindole, oxazole and thiazole. 20 In this class, we prefer that: Q is defined such that a=b=0, c=2 or 3 and n=1;

R

1 , R 2 , R 3 , R 4 each independently represent a coordinating group selected from optionally substituted pyridin-2-yl, optionally substituted imidazol-2-yl, 25 optionally substituted imidazol-4-yl, optionally substituted pyrazol-1-yl, and optionally substituted quinolin-2-yl. (ii) ligands of the general formula (IIB) wherein:

R

1 , R 2 , R 3 each independently represent a coordinating 30 group selected from carboxylate, amido, -NH-C(NH)NH 2 , hydroxyphenyl, an optionally substituted heterocyclic ring WO 01/16271 PCT/EPOO/08076 - 25 or an optionally substituted heteroaromatic ring selected from pyridine, pyrimidine, pyrazine, pyrazole, imidazole, benzimidazole, quinoline, quinoxaline, triazole, isoquinoline, carbazole, indole, isoindole, oxazole and 5 thiazole; and

R

4 represents a group selected from hydrogen, Cl 20 optionally substituted alkyl, Cl 2 0 optionally substituted arylalkyl, aryl, and Ci- 2 0 optionally substituted NR 3 ' (wherein R=C 1 8 -alkyl). 10 In this class, we prefer that: Q is defined such that a=b=0, c=2 or 3 and n=1;

R

1 , R 2 , R 3 each independently represent a coordinating group selected from optionally substituted pyridin-2-yl, 15 optionally substituted imidazol-2-yl, optionally substituted imidazol-4-yl, optionally substituted pyrazol-1-yl, and optionally substituted quinolin-2-yl; and

R

4 represents a group selected from hydrogen, Ci-o optionally substituted alkyl, C 1 5 -furanyl, C 1

-

5 optionally 20 substituted benzylalkyl, benzyl, C1.

5 optionally substituted alkoxy, and Cl- 2 0 optionally substituted N*Me 3 . (iii) ligands of the general formula (IIB) wherein:

R

1 , R 4 each independently represent a coordinating group 25 selected from carboxylate, amido, -NH-C(NH)NH 2 , hydroxyphenyl, an optionally substituted heterocyclic ring or an optionally substituted heteroaromatic ring selected from pyridine, pyrimidine, pyrazine, pyrazole, imidazole, benzimidazole, quinoline, quinoxaline, triazole, 30 isoquinoline, carbazole, indole, isoindole, oxazole and thiazole; and WO 01/16271 PCT/EPOO/08076 - 26 R 2 , R 3 each independently represent a group selected from hydrogen, Cl- 2 0 optionally substituted alkyl, Cl20 optionally substituted arylalkyl, aryl, and Cl 20 optionally substituted NR 3 * (wherein R=C 1 8 -alkyl) 5 In this class, we prefer that: Q is defined such that a=b=0, c=2 or 3 and n=1;

R

1 , R 4 each independently represent a coordinating group selected from optionally substituted pyridin-2-yl, 10 optionally substituted imidazol-2-yl, optionally substituted imidazol-4-yl, optionally substituted pyrazol-1-yl, and optionally substituted quinolin-2-yl; and

R

2 , R 3 each independently represent a group selected from hydrogen, C- 10 optionally substituted alkyl, C 5 15 furanyl, C 1

.

5 optionally substituted benzylalkyl, benzyl, C 1

-

5 optionally substituted alkoxy, and Cl- 20 optionally substituted N*Me 3 . Examples of preferred ligands in their simplest forms are: 20 N,N',N'-tris(3-methyl-pyridin-2-ylmethyl)-ethylenediamine; N-trimethylammoniumpropyl-N,N',N'-tris(pyridin-2-ylmethyl) ethylenediamine; N-(2-hydroxyethylene)-N,N',N'-tris(pyridin-2-ylmethyl) 25 ethylenediamine; N,N,N',N'-tetrakis(3-methyl-pyridin-2-ylmethyl)-ethylene diamine; N,N'-dimethyl-N,N'-bis(pyridin-2-ylmethyl)-cyclohexane-1,2 diamine; 30 N-(2-hydroxyethylene)-N,N',N'-tris(3-methyl-pyridin-2 ylmethyl)-ethylenediamine; WO 01/16271 PCTIEPOO/08076 - 27 N-methyl-N,N' ,N' -tris (pyridin-2-ylmethyl) -ethylenediamine; N-methyl-N,N' ,N' -tris (5-ethyl-pyridin-2-ylmethyl) ethylenediamine; N-methyl-N,N' ,N' -tris(5-methyl-pyridin-2-ylmethyl) 5 ethylenediamine; N-methyl-N,N' ,N' -tris (3-methyl-pyridin-2-ylmethyl) ethylenediamine; N-benzyl-N,N' ,N' -tris (3-methyl-pyridin-2-ylmethyl) ethylenediamine; 10 N-ethyl-N,N' ,N' -tris(3-methyl-pyridin-2-ylmethyl) ethylenediamine; N,N,N' -tris (3-methyl-pyridin-2-ylmethyl) -N'(2' -methaxy ethyl-i) -ethylenediamine; N,N,N' -tris(l-methyl-benzimidazol-2-yl) -N' -methyl 15 ethyl enediamine; N- (furan-2-yl) -N,N' ,N' -tris (3-methyl-pyridin-2-ylmethyl) ethylenediamine; N- (2-hydroxyethylene) -N,N' ,N' -tris (3-ethyl-pyridin-2 ylmethyl) -ethylenediamine; 20 N-methyl-N,N' ,N' -tris (3-methyl-pyridin-2-ylmethyl)ethylene 1, 2-diamine; N-ethyl-N,N' ,N' -tris(3-methyl-pyridiln-2-ylmethyl)ethylele 1,2 -diamine; 25 N-benzyl-N,N' ,N' -tris (3-methyl-pyridin-2-ylmethyl)ethylene 1,2-diamine; N- (2-hydroxyethyl) -N,N' ,N' -tris (3-methyl -pyridin-2 ylmethyl) ethylene-l, 2-diamine; N- (2-methoxyethyl) -N,N' ,N' -tris (3-methyl-pyridin-2 30 ylmethyl) ethylene-l,2-diamine; WO 01/16271 PCT/EPOO/08076 - 28 N-methyl-N,N',N'-tris(5-methyl-pyridin-2-ylmethyl)ethylene 1,2-diamine; N-ethyl-N,N',N'-tris(5-methyl-pyridin-2-ylmethyl)ethylene 1,2-diamine; 5 N-benzyl-N,N',N'-tris(5-methyl-pyridin-2-ylmethyl)ethylene 1,2-diamine; N-(2-hydroxyethyl)-N,N',N'-tris(5-methyl-pyridin-2 ylmethyl)ethylene-1,2-diamine; N-(2-methoxyethyl)-N,N',N'-tris(5-methyl-pyridin-2 10 ylmethyl)ethylene-1,2-diamine; N-methyl-N,N',N'-tris(3-ethyl-pyridin-2-ylmethyl)ethylene 1,2-diamine; N-ethyl-N,N',N'-tris(3-ethyl-pyridin-2-ylmethyl)ethylene 15 1,2-diamine; N-benzyl-N,N',N'-tris(3-ethyl-pyridin-2-ylmethyl)ethylene 1,2-diamine; N-(2-hydroxyethyl)-N,N',N'-tris(3-ethyl-pyridin-2 ylmethyl)ethylene-1,2-diamine; 20 N-(2-methoxyethyl)-N,N',N'-tris(3-ethyl-pyridin-2 ylmethyl)ethylene-1,2-diamine; N-methyl-N,N',N'-tris(5-ethyl-pyridin-2-ylmethyl)ethylene 1,2-diamine; 25 N-ethyl-N,N',N'-tris(5-ethyl-pyridin-2-ylmethyl)ethylene 1,2-diamine; N-benzyl-N,N',N'-tris(5-ethyl-pyridin-2-ylmethyl)ethylene 1,2-diamine; and N-(2-methoxyethyl)-N,N',N'-tris(5-ethyl-pyridin-2 30 ylmethyl)ethylene-1,2-diamine.

WO 01/16271 PCTEP00/08076 - 29 More preferred ligands are: N-methyl-N,N',N'-tris(3-methyl-pyridin-2-ylmethyl)ethylene 1,2-diamine; N-ethyl-N,N',N'-tris(3-methyl-pyridin-2-ylmethyl)ethylene 5 1,2-diamine; N-benzyl-N,N',N'-tris(3-methyl-pyridin-2-ylmethyl)ethylene 1,2-diamine; N-(2-hydroxyethyl)-N,N',N'-tris(3-methyl-pyridin-2 ylmethyl)ethylene-1,2-diamine; and 10 N-(2-methoxyethyl)-N,N',N'-tris(3-methyl-pyridin-2 ylmethyl)ethylene-1,2-diamine. (C) Ligands of the general formula (IC): Q/ Z3 zi I z Z1 N Q1 Q2 15 Z 2 (IC) wherein

Z

1 , Z 2 and Z 3 independently represent a coordinating group selected from carboxylate, amido, -NH-C(NH)NH 2 , 20 hydroxyphenyl, an optionally substituted heterocyclic ring or an optionally substituted heteroaromatic ring selected from pyridine, pyrimidine, pyrazine, pyrazole, imidazole, benzimidazole, quinoline, quinoxaline, triazole, isoquinoline, carbazole, indole, isoindole, oxazole and 25 thiazole; WO 01/16271 PCT/EPOO/08076 - 30 Qi, Q2, and Q3 independently represent a group of the formula: 5 7 b c R6 R8 5 wherein 5 > a+b+c > 1; a=0-5; b=0-5; c=0-5; n=1 or 2; 10 Y independently represents a group selected from -0-, S-, -SO-, -SO 2 -, -C(O)-, arylene, alkylene, heteroarylene, heterocycloalkylene, -(G)P-, -P(O)- and -(G)N- , wherein G is selected from hydrogen, alkyl, aryl, arylalkyl, cycloalkyl, each except hydrogen being optionally 15 substituted by one or more functional groups E; and R5, R6, R7, R8 independently represent a group selected from hydrogen, hydroxyl, halogen, -R and -OR, wherein R represents alkyl, alkenyl, cycloalkyl, heterocycloalkyl, 20 aryl, heteroaryl or a carbonyl derivative group, R being optionally substituted by one or more functional groups E, or R5 together with R6, or R7 together with R8, or both, represent oxygen, or R5 together with R7 and/or independently R6 together 25 with R8, or R5 together with R8 and/or independently R6 WO 01/16271 PCT/EPOO/08076 - 31 together with R7, represent C 16 -alkylene optionally substituted by C 1 4 -alkyl, -F, -Cl, -Br or -I.

Z

1 , Z 2 and Z 3 each represent a coordinating group, preferably 5 selected from optionally substituted pyridin-2-yl, optionally substituted imidazol-2-yl, optionally substituted imidazol-4-yl, optionally substituted pyrazol-1-yl, and optionally substituted quinolin-2-yl. Preferably, Z 1 , Z 2 and

Z

3 each represent optionally substituted pyridin-2-yl. 10 Optional substituents for the groups Zi, Z 2 and Z 3 are preferably selected from C 14 -alkyl, aryl, arylalkyl, heteroaryl, methoxy, hydroxy, nitro, amino, carboxyl, halo, and carbonyl, preferably methyl. 15 Also preferred is that Q1, Q2 and Q3 are defined such that a=b=0, c=1 or 2, and n=1. Preferably, each Q1, Q2 and Q3 independently represent C 1 4 20 alkylene, more preferably a group selected from -CH 2 - and CH 2

CH

2 -. The groups R5, R6, R7, R8 preferably independently represent a group selected from -H, hydroxy-Co-C 20 -alkyl, halo-Co-C 20 25 alkyl, nitroso, formyl-Co-C 20 -alkyl, carboxyl-Co-C 20 -alkyl and esters and salts thereof, carbamoyl-Co-C 20 -alkyl, sulfo-Co

C

20 -alkyl and esters and salts thereof, sulfamoyl-Co-C 20 alkyl, amino-Co-C 20 -alkyl, aryl-Co-C 20 -alkyl, Co-C 20 -alkyl, alkoxy-Co-C 8 -alkyl, carbonyl-Co-C 6 -alkoxy, and Co-C 20 30 alkylamide. Preferably, none of R5-R8 is linked together.

WO 01/16271 PCT/EPOO/08076 - 32 Preferably, the ligand is selected from tris(pyridin-2 ylmethyl)amine, tris(3-methyl-pyridin-2-ylmethyl)amine, tris(5-methyl-pyridin-2-ylmethyl)amine, and tris(6-methyl pyridin-2-ylmethyl)amine. 5 (D) Ligands of the general formula (ID): R1I Q N N Q2R2 I I Q N /03 R3 Q 10 (ID) wherein

R

1 , R 2 , and R 3 independently represent a group selected 15 from hydrogen, hydroxyl, halogen, -NH-C(NH)NH 2 , -R and -OR, wherein R= alkyl, alkenyl, cycloalkyl, heterocycloalkyl, aryl, heteroaryl or a carbonyl derivative group, R being optionally substituted by one or more functional groups E; 20 Q independently represent a group selected from C 2

-

3 alkylene optionally substituted by H, benzyl or C 18 -alkyl;

Q

1 , Q2 and Q 3 independently represent a group of the formula: 25 WO 01/16271 PCT/EPOO/08076 - 33 P5 P 7 ja+ R6 R8 wherein 5 5 > a+b+c > 1; a=0-5; b=0-5; c=0-5; n=1 or 2; Y independently represents a group selected from -0-, S-, -SO-, -SO 2 -, -C(O)-, arylene, alkylene, heteroarylene, heterocycloalkylene, -(G)P-, -P(O)- and -(G)N- , wherein G 10 is selected from hydrogen, alkyl, aryl, arylalkyl, cycloalkyl, each except hydrogen being optionally substituted by one or more functional groups E; and R5, R6, R7, R8 independently represent a group selected 15 from hydrogen, hydroxyl, halogen, -R and -OR, wherein R represents alkyl, alkenyl, cycloalkyl, heterocycloalkyl, aryl, heteroaryl or a carbonyl derivative group, R being optionally substituted by one or more functional groups E, or R5 together with R6, or R7 together with R8, or 20 both, represent oxygen, or R5 together with R7 and/or independently R6 together with R8, or R5 together with R8 and/or independently R6 together with R7, represent Ci-6-alkylene optionally substituted by C 1 4 -alkyl, -F, -Cl, -Br or -I, 25 WO 01/16271 PCT/EPOO/08076 - 34 provided that at least one, preferably at least two, of

R

1 , R 2 and R 3 is a coordinating group. At least two, and preferably at least three, of RI, R 2 and R 3 5 independently represent a group selected from carboxylate, amido, -NH-C(NH)NH 2 , hydroxyphenyl, an optionally substituted heterocyclic ring or an optionally substituted heteroaromatic ring selected from pyridine, pyrimidine, pyrazine, pyrazole, imidazole, benzimidazole, quinoline, 10 quinoxaline, triazole, isoquinoline, carbazole, indole, isoindole, oxazole and thiazole. Preferably, at least two of R 1 , R 2 , R 3 each independently represent a coordinating group selected from optionally substituted pyridin-2-yl, optionally substituted imidazol-2-yl, optionally substituted 15 imidazol-4-yl, optionally substituted pyrazol-1-yl, and optionally substituted quinolin-2-yl. Preferably, substituents for groups R 1 , R 2 , R 3 , when representing a heterocyclic or heteroaromatic ring, are 20 selected from C 14 -alkyl, aryl, arylalkyl, heteroaryl, methoxy, hydroxy, nitro, amino, carboxyl, halo, and carbonyl. Preferably, Q 1 , Q2 and Q3 are defined such that a=b=O, c=1,2,3 or 4 and n=1. Preferably, the groups Qi, Q2 and Q3 25 independently represent a group selected from -CH 2 - and CH 2

CH

2 -. Group Q is preferably a group selected from -CH 2

CH

2 - and CH 2C H2 CH2 -. 30 WO 01/16271 PCT/EPOO/08076 - 35 The groups R5, R6, R7, R8 preferably independently represent a group selected from -H, hydroxy-Co-C 20 -alkyl, halo-Co-C 2 0 alkyl, nitroso, formyl-Co-C 20 -alkyl, carboxyl-Co-C 20 -alkyl and esters and salts thereof, carbamoyl-Co-C 20 -alkyl, sulfo-Co 5 C 2 0-alkyl and esters and salts thereof, sulfamoyl-C-C 20 alkyl, amino-Co-C 2 0 -alkyl, aryl-Co-C 20 -alkyl, Co-C 20 -alkyl, alkoxy-Co-C 8 -alkyl, carbonyl-Co-C 6 -alkoxy, and Co-C 2 0 alkylamide. Preferably, none of R5-R8 is linked together. 10 In a preferred aspect, the ligand is of the general formula (IID): Q--R2 N R1-Q N R3 (IID) 15 wherein R1, R2, R3 are as defined previously for R 1 , R 2 , R 3 , and Q1, Q2, Q3 are as defined previously. Preferred classes of ligands according to this preferred 20 aspect, as represented by formula (IID) above, are as follows: (i) ligands of the general formula (IID) wherein: R1, R2, R3 each independently represent a coordinating 25 group selected from carboxylate, amido, -NH-C(NH)NH 2

,

WO 01/16271 PCT/EPOO/08076 - 36 hydroxyphenyl, an optionally substituted heterocyclic ring or an optionally substituted heteroaromatic ring selected from pyridine, pyrimidine, pyrazine, pyrazole, imidazole, benzimidazole, quinoline, quinoxaline, triazole, 5 isoquinoline, carbazole, indole, isoindole, oxazole and thiazole. In this class, we prefer that: R1, R2, R3 each independently represent a coordinating 10 group selected from optionally substituted pyridin-2-yl, optionally substituted imidazol-2-yl, optionally substituted imidazol-4-yl, optionally substituted pyrazol-1-yl, and optionally substituted quinolin-2-yl. 15 (ii) ligands of the general formula (IID) wherein: two of R1, R2, R3 each independently represent a coordinating group selected from carboxylate, amido, -NH

C(NH)NH

2 , hydroxyphenyl, an optionally substituted heterocyclic ring or an optionally substituted 20 heteroaromatic ring selected from pyridine, pyrimidine, pyrazine, pyrazole, imidazole, benzimidazole, quinoline, quinoxaline, triazole, isoquinoline, carbazole, indole, isoindole, oxazole and thiazole; and one of R1, R2, R3 represents a group selected from 25 hydrogen, Cl 20 optionally substituted alkyl, Cl 2 0 optionally substituted arylalkyl, aryl, and Cl- 2 0 optionally substituted

NR

3 + (wherein R=C 1 e-alkyl). In this class, we prefer that: 30 two of R1, R2, R3 each independently represent a coordinating group selected from optionally substituted WO 01/16271 PCT/EPOO/08076 - 37 pyridin-2-yl, optionally substituted imidazol-2-yl, optionally substituted imidazol-4-yl, optionally substituted pyrazol-1-yl, and optionally substituted quinolin-2-yl; and one of R1, R2, R3 represents a group selected from 5 hydrogen, Ci-io optionally substituted alkyl, C 1 5 -furanyl, C 1

-

5 optionally substituted benzylalkyl, benzyl, Ci-s optionally substituted alkoxy, and C 1

-

2 0 optionally substituted N*Me 3 . In especially preferred embodiments, the ligand is selected 10 from: Pz3 N -N N Pz3 Pzl N Pzl N Q N N Pzl N Pzy N Pzl N N Et Et wherein -Et represents ethyl, -Py represents pyridin-2-yl, 15 Pz3 represents pyrazol-3-yl, Pzl represents pyrazol-1-yl, and Qu represents quinolin-2-yl.

WO 01/16271 PCT/EPOO/08076 - 38 (E) Ligands of the general formula (IE): T1- [-N- (Q1) r- s-N- (Q2) g-T2 5 R1 R2 (IE) wherein g represents zero or an integer from 1 to 6; 10 r represents an integer from 1 to 6; s represents zero or an integer from 1 to 6; Q1 and Q2 independently represent a group of the formula: 15 6 8 - -C d- [-Y1-] e- [-C- e R7 R9 wherein 20 5 > d+e+f > 1; d=0-5; e=0-5; f=0-5; each Y1 independently represents a group selected from -0-, -S-, -SO-, -S02-, -C(O)-, arylene, alkylene, heteroarylene, heterocycloalkylene, -(G)P-, -P(O)- and (G)N- , wherein G is selected from hydrogen, alkyl, aryl, 25 arylalkyl, cycloalkyl, each except hydrogen being optionally substituted by one or more functional groups E; if s>1, each - [-N(Rl) - (Q1)r-] - group is independently defined; 30 WO 01/16271 PCT/EPOO/08076 - 39 R1, R2, R6, R7, R8, R9 independently represent a group selected from hydrogen, hydroxyl, halogen, -R and -OR, wherein R represents alkyl, alkenyl, cycloalkyl, heterocycloalkyl, aryl, heteroaryl or a carbonyl derivative 5 group, R being optionally substituted by one or more functional groups E, or R6 together with R7, or R8 together with R9, or both, represent oxygen, or R6 together with R8 and/or independently R7 together 10 with R9, or R6 together with R9 and/or independently R7 together with R8, represent C 1 .s-alkylene optionally substituted by C 1

.

4 -alkyl, -F, -Cl, -Br or -I; or one of R1-R9 is a bridging group bound to another moiety of the same general formula; 15 T1 and T2 independently represent groups R4 and R5, wherein R4 and R5 are as defined for Rl-R9, and if g=0 and s>0, R1 together with R4, and/or R2 together with R5, may optionally independently represent =CH-R10, wherein R10 is 20 as defined for Rl-R9, or T1 and T2 may together (-T2-Tl-) represent a covalent bond linkage when s>1 and g>0; if T1 and T2 together represent a single bond linkage, 25 Q1 and/or Q2 may independently represent a group of the formula: =CH-I[-Y-]e-CH= provided R1 and/or R2 are absent, and R1 and/or R2 may be absent provided Q1 and/or Q2 independently represent a group of the formula: =CH- [-Y1-] e-CH=. 30 WO 01/16271 PCT/EPOO/08076 - 40 The groups R1-R9 are preferably independently selected from -H, hydroxy-Co-C 20 -alkyl, halo-Co-C 20 -alkyl, nitroso, formyl Co-C 20 -alkyl, carboxyl-Co-C 20 -alkyl and esters and salts thereof, carbamoyl-Co-C 20 -alkyl, sulpho-Co-C 20 -alkyl and 5 esters and salts thereof, sulphamoyl-Co-C 20 -alkyl, amino-Co

C

20 -alkyl, aryl-Co-C 20 -alkyl, heteroaryl-Co-C 20 -alkyl, Co-C 2 0 alkyl, alkoxy-Co-Cs-alkyl, carbonyl-Co-Cs-alkoxy, and aryl-Co

C

6 -alkyl and Co-C 20 -alkylamide. 10 One of R1-R9 may be a bridging group which links the ligand moiety to a second ligand moiety of preferably the same general structure. In this case the bridging group is independently defined according to the formula for Q1, Q2, preferably being alkylene or hydroxy-alkylene or a 15 heteroaryl-containing bridge, more preferably C 1

-

6 -alkylene optionally substituted by C 14 -alkyl, -F, -Cl, -Br or -I. In a first variant according to formula (IE), the groups T1 and T2 together form a single bond linkage and s>1, 20 according to general formula (IIE): R3\ N~I) (13)R R1

(IIE)

WO 01/16271 PCT/EPOO/08076 - 41 wherein R3 independently represents a group as defined for R1-R9; Q3 independently represents a group as defined for Q1, Q2; h represents zero or an integer from 1 to 6; and s=s-1. 5 In a first embodiment of the first variant, in general formula (IIE), s=1, 2 or 3; r=g=h=1; d=2 or 3; e=f=O; R6=R7=H, preferably such that the ligand has a general formula selected from: WO 01/16271 PCT/EPOO/08076 - 42 R1 R1 I R1 N-R3 N-R3 N-R3 R2 R2 R2 R1 N R1 N NR2 R1 \R2 N-R3N N N 10 C N N-3 KN N 9 /IN N" R2 R4 R3 R4 R3 R1 R2 N N R5.N N R3 R4 20 In these preferred examples, R1, R2, R3 and R4 are preferably independently selected from -H, alkyl, aryl, heteroaryl, and/or one of R1-R4 represents a bridging group bound to another moiety of the same general formula and/or two or more of R1-R4 together represent a bridging group 25 linking N atoms in the same moiety, with the bridging group being alkylene or hydroxy-alkylene or a heteroaryl containing bridge, preferably heteroarylene. More preferably, R1, R2, R3 and R4 are independently selected from -H, methyl, ethyl, isopropyl, nitrogen-containing 30 heteroaryl, or a bridging group bound to another moiety of the same general formula or linking N atoms in the same WO 01/16271 PCT/EPOO/08076 - 43 moiety with the bridging group being alkylene or hydroxy alkylene. In a second embodiment of the first variant, in general 5 formula (IIE), s=2 and r=g=h=l, according to the general formula: , q-N QZ /N--Ql R1 In this second embodiment, preferably R1-R4 are absent; both 10 Q1 and Q3 represent =CH- [-Y1-],-CH= ; and both Q2 and Q4 represent -CH 2 - [-Y1- n-CH 2

-

Thus, preferably the ligand has the general formula: R5 -N N- R4

R

1 OH HO / R 2 -N N- R3 A n 15 wherein A represents optionally substituted alkylene optionally interrupted by a heteroatom; and n is zero or an integer from 1 to 5.

WO 01/16271 PCT/EP00/08076 - 44 Preferably, R1-R6 represent hydrogen, n=1 and A= -CH 2 -, CHOH-, -CH 2

N(R)CH

2 - or -CH 2

CH

2

N(R)CH

2

CH

2 - wherein R represents hydrogen or alkyl, more preferably A= -CH 2 -, -CHOH- or CH 2

CH

2

NHCH

2

CH

2 5 In a second variant according to formula (IE) , T1 and T2 independently represent groups R4, R5 as defined for Rl-R9, according to the general formula (IIIE): 10 R4- [-V- (Q1) r-] s-V- (Q 2 ) g-R5 R1 R2 (IIIE) In a first embodiment of the second variant, in general 15 formula (IIIE) , s=1; r=1; g=O; d=f=1; e=0-4; Y1= -CH 2 -; and R1 together with R4, and/or R2 together with R5, independently represent =CH-R10, wherein R10 is as defined for Rl-R9. In one example, R2 together with R5 represents =CH-R1O, with R1 and R4 being two separate groups. 20 Alternatively, both R1 together with R4, and R2 together with R5 may independently represent =CH-RlO. Thus, preferred ligands may for example have a structure selected from: R2 R3 R2 R3 R CH 2

R

5 Re CH 2 1 -R5 ni n N N== R 7 -N N== R1 R4 IR4 25 wherein n = 0-4.

WO 01/16271 PCT/EPOO/08076 - 45 Preferably, the ligand is selected from: =-N N== R 4 -N N R1 R2 IR1 1

R

3 5 wherein Rland R2 are selected from optionally substituted phenols, heteroaryl-Co-C 20 -alkyls, R3 and R4 are selected from -H, alkyl, aryl, optionally substituted phenols, heteroaryl-Co-C 20 -alkyls, alkylaryl, aminoalkyl, alkoxy, more preferably Ri and R2 being selected from optionally 10 substituted phenols, heteroaryl-Co-C 2 -alkyls, R3 and R4 are selected from -H, alkyl, aryl, optionally substituted phenols, nitrogen-heteroaryl-Co-C 2 -alkyls. In a second embodiment of the second variant, in general 15 formula (IIIE) , s=1; r=1; g=0; d=f=1; e=1-4; Y1= -C(R') (R") wherein R' and R" are independently as defined for Rl-R9. Preferably, the ligand has the general formula:

R

2 R5 R3 20 RI R4 R7-N R6 N-R9 R8 RIO The groups R1, R2, R3, R4, R5 in this formula are preferably 25 -H or Co-C 20 -alkyl, n=0 or 1, R6 is -H, alkyl, -OH or -SH, and R7, R8, R9, R10 are preferably each independently selected from -H, Co-C 20 -alkyl, heteroaryl-Co-C 20 -alkyl, alkoxy-Co-CB-alkyl and amino-Co-C 20 -alkyl.

WO 01/16271 PCT/EPOO/08076 - 46 In a third embodiment of the second variant, in general formula (IIIE), s=0; g=1; d=e=0; f=1-4. Preferably, the ligand has the general formula: 5 R2 RI R3 R4 N'R5 This class of ligand is particularly preferred according to 10 the invention. More preferably, the ligand has the general formula: RI 1 N N' R2-* N R3 15 wherein R1, R2, R3 are as defined for R2, R4, R5. In a fourth embodiment of the second variant, the ligand is a pentadentate ligand of the general formula (IVE):

R

3 -- C-N 20 R1 R 2 (IVE) wherein each R 1 , R 2 independently represents -R 4 -Rs, WO 01/16271 PCT/EPOO/08076 - 47 R3 represents hydrogen, optionally substituted alkyl, aryl or arylalkyl, or -R 4

-R

5 , each R 4 independently represents a single bond or optionally substituted alkylene, alkenylene, oxyalkylene, 5 aminoalkylene, alkylene ether, carboxylic ester or carboxylic amide, and each R 5 independently represents an optionally N substituted aminoalkyl group or an optionally substituted heteroaryl group selected from pyridinyl, pyrazinyl, 10 pyrazolyl, pyrrolyl, imidazolyl, benzimidazolyl, pyrimidinyl, triazolyl and thiazolyl. Ligands of the class represented by general formula (IVE) are also particularly preferred according to the invention. 15 The ligand having the general formula (IVE), as defined above, is a pentadentate ligand. By 'pentadentate' herein is meant that five hetero atoms can coordinate to the metal M ion in the metal-complex. 20 In formula (IVE), one coordinating hetero atom is provided by the nitrogen atom in the methylamine backbone, and preferably one coordinating hetero atom is contained in each of the four R 1 and R 2 side groups. Preferably, all the coordinating hetero atoms are nitrogen atoms. 25 The ligand of formula (IVE) preferably comprises at least two substituted or unsubstituted heteroaryl groups in the four side groups. The heteroaryl group is preferably a pyridin-2-yl group and, if substituted, preferably a methyl 30 or ethyl-substituted pyridin-2-yl group. More preferably, the heteroaryl group is an unsubstituted pyridin-2-yl group.

WO 01/16271 PCT/EPOO/08076 - 48 Preferably, the heteroaryl group is linked to methylamine, and preferably to the N atom thereof, via a methylene group. Preferably, the ligand of formula (IVE) contains at least one optionally substituted amino-alkyl side group, more 5 preferably two amino-ethyl side groups, in particular 2-(N alkyl)amino-ethyl or 2-(N,N-dialkyl)amino-ethyl. Thus, in formula (IVE) preferably R 1 represents pyridin-2-yl or R 2 represents pyridin-2-yl-methyl. Preferably R 2 or R1 10 represents 2-amino-ethyl, 2-(N-(m)ethyl)amino-ethyl or 2 (N,N-di(m)ethyl)amino-ethyl. If substituted, R5 preferably represents 3-methyl pyridin-2-yl. R 3 preferably represents hydrogen, benzyl or methyl. 15 Examples of preferred ligands of formula (IVE) in their simplest forms are: (i) pyridin-2-yl containing ligands such as: N,N-bis(pyridin-2-yl-methyl)-bis(pyridin-2-yl)methylamine; 20 N,N-bis(pyrazol-1-yl-methyl)-bis(pyridin-2-yl)methylamine; N,N-bis(imidazol-2-yl-methyl)-bis(pyridin-2-yl)methylamine; N,N-bis(1,2,4-triazol-1-yl-methyl)-bis(pyridin-2 yl)methylamine; N,N-bis(pyridin-2-yl-methyl)-bis(pyrazol-1-yl)methylamine; 25 N,N-bis(pyridin-2-yl-methyl)-bis(imidazol-2-yl)methylamine; N,N-bis(pyridin-2-yl-methyl)-bis(1,2,4-triazol-l yl)methylamine; N,N-bis(pyridin-2-yl-methyl)-1,1-bis(pyridin-2-yl)-1 aminoethane; 30 N,N-bis(pyridin-2-yl-methyl)-1,1-bis(pyridin-2-yl)-2-phenyl 1-aminoethane; WO 01/16271 PCTIEPOO/08076 - 49 N,N-bis (pyrazol-1-yl -methyl) -1, 1-bis (pyridin-2-yl) -1 aminoethane; N,N-bis(pyrazol-l-y1-methyl) -1,1-bis(pyridin-2-yl) -2-phenyl 1-aminoethane; 5 N,N-bis(imidazol-2-yl-nethyl) -1,l-bis(pyridin-2-yl) -1 aminoethane; N,N-bis(imidazol-2-yl-methyl) -1,l-bis(pyridin-2-yl) -2 phenyl -1-aminoethane; N,N-bis(l,2,4-triazol-l-yl-methyl)-1,1-bis(pyridin-2-yl)-1 10 aminoethane; N,N-bis(1,2,4-triazol-l-yl-methyl)-l,1-bis(pyridin-2-yl)-2 phenyl -1-aminoethane; N,N-bis (pyridin-2-yl-methyl) -1, 1-bis (pyrazol-1-y1) -1 aminoethane; 15 N,N-bis (pyridin-2-y1-methyl) -1, 1-bis (pyrazol-1-yl) -2-phenyl 1-aminoethane; N,N-bis (pyridin-2-y1-methyl) -1, 1-bis (imidazol-2-yl) -1 aminoethane; N,N-bis(pyridin-2-y1-methyl) -1,1-bis(imidazol-2-y1) -2 20 phenyl -1-aminoethane; N,N-bis(pyridin-2-.yl-methyl)-1,1-bis(1,2,4-triazol-l-yl)-1 aminoethane; N,N-bis(pyridin-2-yl-methyl)-1,1-bis(1,2,4-triazol-1-yl)-1 aminoethane; 25 N,N-bis(pyridin-2-yl-methyl) -1,1-bis(pyridin-2-yl) -1 aminoethane; N,N-bis(pyridin-2-yl-methyl) -1,1-bis(pyridin-2-yl) -1 arninohexane; N,N-bis (pyridin-2-yl-methyl) -1, 1-bis (pyridin-2-y1) -2-phenyl 30 1-aminoethane; WO 01/16271 PCT/EPOO/08076 - 50 N,N-bis(pyridin-2-yl-methyl)-1,1-bis(pyridin-2-yl)-2-(4 sulphonic acid-phenyl)-1-aminoethane; N,N-bis(pyridin-2-yl-methyl)-1,1-bis(pyridin-2-yl)-2 (pyridin-2-yl)-1-aminoethane; 5 N,N-bis(pyridin-2-yl-methyl)-1,1-bis(pyridin-2-yl)-2 (pyridin-3-yl)-1-aminoethane; N,N-bis(pyridin-2-yl-methyl)-1,1-bis(pyridin-2-yl)-2 (pyridin-4-yl)-1-aminoethane; N,N-bis(pyridin-2-yl-methyl)-1,1-bis(pyridin-2-yl)-2-(1 10 alkyl-pyridinium-4-yl)-1-aminoethane; N,N-bis(pyridin-2-yl-methyl)-1,1-bis(pyridin-2-yl)-2-(1 alkyl-pyridinium-3-yl)-1-aminoethane; N,N-bis(pyridin-2-yl-methyl)-1,1-bis(pyridin-2-yl)-2-(1 alkyl-pyridinium-2-yl)-1-aminoethane; 15 (ii) 2-amino-ethyl containing ligands such as: N,N-bis(2-(N-alkyl)amino-ethyl)-bis(pyridin-2 yl)methylamine; N,N-bis(2-(N-alkyl)amino-ethyl)-bis(pyrazol-l 20 yl)methylamine; N,N-bis(2-(N-alkyl)amino-ethyl)-bis(imidazol-2 yl)methylamine; N,N-bis(2-(N-alkyl)amino-ethyl)-bis(1,2,4-triazol-1 yl)methylamine; 25 N,N-bis(2-(N,N-dialkyl)amino-ethyl)-bis(pyridin-2 yl)methylamine; N,N-bis(2-(N,N-dialkyl)amino-ethyl)-bis(pyrazol-l yl)methylamine; N,N-bis(2-(N,N-dialkyl)amino-ethyl)-bis(imidazol-2 30 yl)methylamine; WO 01/16271 PCT/EPOO/08076 - 51 N,N-bis(2-(N,N-dialkyl)amino-ethyl)-bis(1,2,4-triazol-1 yl)methylamine; N,N-bis(pyridin-2-yl-methyl)-bis(2-amino-ethyl)methylamine; N,N-bis(pyrazol-l-yl-methyl)-bis(2-amino-ethyl)methylamine; 5 N,N-bis(imidazol-2-yl-methyl)-bis(2-amino-ethyl)methylamine; N,N-bis(1,2,4-triazol-1-yl-methyl)-bis(2-amino ethyl)methylamine. More preferred ligands are: 10 N,N-bis(pyridin-2-yl-methyl)-bis(pyridin-2-yl)methylamine, hereafter referred to as N4Py. N,N-bis(pyridin-2-yl-methyl)-1,1-bis(pyridin-2-yl)-1 aminoethane, hereafter referred to as MeN4Py, N,N-bis(pyridin-2-yl-methyl)-1,1-bis(pyridin-2-yl)-2-phenyl 15 1-aminoethane, hereafter referred to as BzN4Py. In a fifth embodiment of the second variant, the ligand represents a pentadentate or hexadentate ligand of general formula (VE): 20

R

1

R'N-W-NR'R

2 (VE) wherein 25 each R1 independently represents -R -V, in which R 3 represents optionally substituted alkylene, alkenylene, oxyalkylene, aminoalkylene or alkylene ether, and V represents an optionally substituted heteroaryl group selected from pyridinyl, pyrazinyl, pyrazolyl, pyrrolyl, 30 imidazolyl, benzimidazolyl, pyrimidinyl, triazolyl and thiazolyl; WO 01/16271 PCT/EPOO/08076 - 52 W represents an optionally substituted alkylene bridging group selected from

-CH

2

CH

2 -, -CH 2

CH

2

CH

2 -, -CH 2

CH

2

CH

2

CH

2 -, -CH 2

-C

6

H

4

-CH

2 -, -CH 2

-C

6 Hio

CH

2 -, and -CH 2

-C

10

H

6

-CH

2 -; and 5 R 2 represents a group selected from R', and alkyl, aryl and arylalkyl groups optionally substituted with a substituent selected from hydroxy, alkoxy, phenoxy, carboxylate, carboxamide, carboxylic ester, sulphonate, amine, alkylamine and N*(R 4

)

3 , wherein R 4 is selected from 10 hydrogen, alkanyl, alkenyl, arylalkanyl, arylalkenyl, oxyalkanyl, oxyalkenyl, aminoalkanyl, aminoalkenyl, alkanyl ether and alkenyl ether. The ligand having the general formula (VE), as defined 15 above, is a pentadentate ligand or, if R-=R 2 , can be a hexadentate ligand. As mentioned above, by 'pentadentate' is meant that five hetero atoms can coordinate to the metal M ion in the metal-complex. Similarly, by 'hexadentate' is meant that six hetero atoms can in principle coordinate to 20 the metal M ion. However, in this case it is believed that one of the arms will not be bound in the complex, so that the hexadentate ligand will be penta coordinating. In the formula (yE), two hetero atoms are linked by the 25 bridging group W and one coordinating hetero atom is contained in each of the three R 1 groups. Preferably, the coordinating hetero atoms are nitrogen atoms. The ligand of formula (VE) comprises at least one optionally 30 substituted heteroaryl group in each of the three R 1 groups. Preferably, the heteroaryl group is a pyridin-2-yl group, in WO 01/16271 PCT/EPOO/08076 - 53 particular a methyl- or ethyl-substituted pyridin-2-yl group. The heteroaryl group is linked to an N atom in formula (VE), preferably via an alkylene group, more preferably a methylene group. Most preferably, the 5 heteroaryl group is a 3-methyl-pyridin-2-yl group linked to an N atom via methylene. The group R 2 in formula (VE) is a substituted or unsubstituted alkyl, aryl or arylalkyl group, or a group R 1 . 10 However, preferably R 2 is different from each of the groups R1 in the formula above. Preferably, R 2 is methyl, ethyl, benzyl, 2-hydroxyethyl or 2-methoxyethyl. More preferably,

R

2 is methyl or ethyl. 15 The bridging group W may be a substituted or unsubstituted alkylene group selected from -CH 2

CH

2 -, -CH 2

CH

2

CH

2 -, -CH 2

CH

2

CH

2

CH

2 -, -CH 2

-C

6

H

4

-CH

2 -, -CH 2

-C

6 Hio-CH 2 -, and -CH 2 -CioH 6

-CH

2 (wherein -C 6

H

4 -, -C 6 Hio-, -CioH- 6 can be ortho-, para-, or meta-C 6

H

4 -, -C 6 Hio-, -CioH 6 -) . Preferably, the bridging group 20 W is an ethylene or 1,4-butylene group, more preferably an ethylene group. Preferably, V represents substituted pyridin-2-yl, especially methyl-substituted or ethyl-substituted pyridin 25 2-yl, and most preferably V represents 3-methyl pyridin-2 yl. (F) Ligands of the classes disclosed in WO-A-98/39098 and WO-A-98/39406. 30 WO 01/16271 PCT/EPOO/08076 - 54 The counter ions Y in formula (Al) balance the charge z on the complex formed by the ligand L, metal M and coordinating species X. Thus, if the charge z is positive, Y may be an anion such as RCOO~, BPh 4 ~, C10 4 ~, BF 4 ~, PF6~, RSO3~, RS0 4 ~, S0 4 2 5 , N0 3 -, F~, Cl~, Br-, or I~, with R being hydrogen, optionally substituted alkyl or optionally substituted aryl. If z is negative, Y may be a common cation such as an alkali metal, alkaline earth metal or (alkyl)ammonium cation. 10 Suitable counter ions Y include those which give rise to the formation of storage-stable solids. Preferred counter ions for the preferred metal complexes are selected from R 7 COO~, C10 4 -, BF 4 , PF6 , RS0 3 (in particular CF 3 SO3) , RSO4, S0 4 2 -, N0 3 ~, F~, Cl~, Br~, and I~, wherein R represents hydrogen or 15 optionally substituted phenyl, naphthyl or C 1

-C

4 alkyl. It will be appreciated that the complex (Al) can be formed by any appropriate means, including in situ formation whereby precursors of the complex are transformed into the 20 active complex of general formula (Al) under conditions of storage or use. Preferably, the complex is formed as a well-defined complex or in a solvent mixture comprising a salt of the metal M and the ligand L or ligand L-generating species. Alternatively, the catalyst may be formed in situ 25 from suitable precursors for the complex, for example in a solution or dispersion containing the precursor materials. In one such example, the active catalyst may be formed in situ in a mixture comprising a salt of the metal M and the ligand L, or a ligand L-generating species, in a suitable 30 solvent. Thus, for example, if M is iron, an iron salt such as FeSO 4 can be mixed in solution with the ligand L, or a WO 01/16271 PCT/EPOO/08076 - 55 ligand L-generating species, to form the active complex. Thus, for example, the composition may formed from a mixture of the ligand L and a metal salt MX, in which preferably n=l 5, more preferably 1-3. In another such example, the ligand 5 L, or a ligand L-generating species, can be mixed with metal M ions present in the substrate or wash liquor to form the active catalyst in situ. Suitable ligand L-generating species include metal-free compounds or metal coordination complexes that comprise the ligand L and can be substituted 10 by metal M ions to form the active complex according the formula (Al). Throughout the description and claims generic groups have been used, for example alkyl, alkoxy, aryl. Unless 15 otherwise specified the following are preferred group restrictions that may be applied to generic groups found within compounds disclosed herein: alkyl: C1-C6-alkyl, 20 alkenyl: C2-C6-alkenyl, cycloalkyl: C3-C8-cycloalkyl, 25 alkoxy: Cl-C6-alkoxy, alkylene: selected from the group consisting of: methylene; 1,1-ethylene; 1,2-ethylene; 1,1-propylene; 1,2-propylene; 1,3-propylene; 2,2-propylene; butan-2-ol-1,4-diyl; propan-2 30 ol-1,3-diyl; and 1,4-butylene, WO 01/16271 PCT/EPOO/08076 - 56 aryl: selected from homoaromatic compounds having a molecular weight under 300, arylene: selected from the group consisting of: 1,2 5 benzene; 1,3-benzene; 1,4-benzene; 1,2-naphthalene; 1,3 naphthalene; 1,4-naphthalene; 2,3-naphthalene; phenol-2,3 diyl; phenol-2,4-diyl; phenol-2,5-diyl; and phenol-2,-6 diyl, 10 heteroaryl: selected from the group consisting of: pyridinyl; pyrimidinyl; pyrazinyl; triazolyl, pyridazinyl; 1,3,5-triazinyl; quinolinyl; isoquinolinyl; quinoxalinyl; imidazolyl; pyrazolyl; benzimidazolyl; thiazolyl; oxazolidinyl; pyrrolyl; carbazolyl; indolyl; and isoindolyl, 15 heteroarylene: selected from the group consisting of: pyridin-2,3-diyl; pyridin-2,4-diyl; pyridin-2,5-diyl; pyridin-2,6-diyl; pyridin-3,4-diyl; pyridin-3,5-diyl; quinolin-2,3-diyl; quinolin-2,4-diyl; quinolin-2,8-diyl; 20 isoquinolin-1,3-diyl; isoquinolin-1,4-diyl; pyrazol-1,3 diyl; pyrazol-3,5-diyl; triazole-3,5-diyl; triazole-1,3 diyl; pyrazin-2,5-diyl; and imidazole-2,4-diyl, heterocycloalkyl: selected from the group consisting of: pyrrolinyl; pyrrolidinyl; morpholinyl; piperidinyl; 25 piperazinyl; hexamethylene imine; and oxazolidinyl, amine: the group -N(R) 2 wherein each R is independently selected from: hydrogen; C1-C6-alkyl; C1-C6-alkyl-C6H5; and phenyl, wherein when both R are C1-C6-alkyl both R together 30 may form an -NC3 to an -NC5 heterocyclic ring with any WO 01/16271 PCT/EPOO/08076 - 57 remaining alkyl chain forming an alkyl substituent to the heterocyclic ring, halogen: selected from the group consisting of: F; Cl; Br 5 and I, sulphonate: the group -S(0) 2 0R, wherein R is selected from: hydrogen; C1-C6-alkyl; phenyl; C1-C6-alkyl-C6H5; Li; Na; K; Cs; Mg; and Ca, 10 sulphate: the group -OS(0) 2 0R, wherein R is selected from: hydrogen; Cl-C6-alkyl; phenyl; C1-C6-alkyl-C6H5; Li; Na; K; Cs; Mg; and Ca, 15 sulphone: the group -S(0) 2 R, wherein R is selected from: hydrogen; C1-C6-alkyl; phenyl; C1-C6-alkyl-C6H5 and amine (to give sulphonamide) selected from the group: -NR'2, wherein each R' is independently selected from: hydrogen; C1-C6-alkyl; Cl-C6-alkyl-C6H5; and phenyl, wherein when both 20 R' are Cl-C6-alkyl both R' together may form an -NC3 to an NC5 heterocyclic ring with any remaining alkyl chain forming an alkyl substituent to the heterocyclic ring, carboxylate derivative: the group -C(O)OR, wherein R is 25 selected from: hydrogen, Cl-C6-alkyl; phenyl; Cl-C6-alkyl C6H5, Li; Na; K; Cs; Mg; and Ca, carbonyl derivative: the group -C(O)R, wherein R is selected from: hydrogen; Cl-C6-alkyl; phenyl; Cl-C6-alkyl 30 C6H5 and amine (to give amide) selected from the group: NR'2, wherein each R' is independently selected from: WO 01/16271 PCT/EPOO/08076 - 58 hydrogen; C1-C6-alkyl; Cl-C6-alkyl-C6H5; and phenyl, wherein when both R' are Cl-C6-alkyl both R' together may form an NC3 to an -NC5 heterocyclic ring with any remaining alkyl chain forming an alkyl substituent to the heterocyclic ring, 5 phosphonate: the group -P(0) (OR) 2 , wherein each R is independently selected from: hydrogen; Cl-C6-alkyl; phenyl; C1-C6-alkyl-C6H5; Li; Na; K; Cs; Mg; and Ca, 10 phosphate: the group -OP(O) (OR) 2 , wherein each R is independently selected from: hydrogen; Cl-C6-alkyl; phenyl; Cl-C6-alkyl-C6H5; Li; Na; K; Cs; Mg; and Ca, phosphine: the group -P(R) 2 , wherein each R is 15 independently selected from: hydrogen; Cl-C6-alkyl; phenyl; and C1-C6-alkyl-C6H5, phosphine oxide: the group -P(O)R 2 , wherein R is independently selected from: hydrogen; Cl-C6-alkyl; phenyl; 20 and Cl-C6-alkyl-C6H5; and amine (to give phosphonamidate) selected from the group: -NR'2, wherein each R' is independently selected from: hydrogen; Cl-C6-alkyl; C1-C6 alkyl-C6H5; and phenyl, wherein when both R' are Cl-C6-alkyl both R' together may form an -NC3 to an -NC5 heterocyclic 25 ring with any remaining alkyl chain forming an alkyl substituent to the heterocyclic ring. Unless otherwise specified the following are more preferred group restrictions that may be applied to groups found 30 within compounds disclosed herein: WO 01/16271 PCT/EPOO/08076 - 59 alkyl: Cl-C4-alkyl, alkenyl: C3-C6-alkenyl, 5 cycloalkyl: C6-C8-cycloalkyl, alkoxy: Cl-C4-alkoxy, alkylene: selected from the group consisting of: methylene; 10 1,2-ethylene; 1,3-propylene; butan-2-ol-1,4-diyl; and 1,4 butylene, aryl: selected from group consisting of: phenyl; biphenyl, naphthalenyl; anthracenyl; and phenanthrenyl, 15 arylene: selected from the group consisting of: 1,2 benzene, 1,3-benzene, 1,4-benzene, 1,2-naphthalene, 1,4 naphthalene, 2,3-naphthalene and phenol-2,6-diyl, 20 heteroaryl: selected from the group consisting of: pyridinyl; pyrimidinyl; quinolinyl; pyrazolyl; triazolyl; isoquinolinyl; imidazolyl; and oxazolidinyl, heteroarylene: selected from the group consisting of: 25 pyridin-2,3-diyl; pyridin-2,4-diyl; pyridin-2,6-diyl; pyridin-3,5-diyl; quinolin-2,3-diyl; quinolin-2,4-diyl; isoquinolin-1,3-diyl; isoquinolin-1,4-diyl; pyrazol-3,5 diyl; and imidazole-2,4-diyl, 30 heterocycloalkyl: selected from the group consisting of: pyrrolidinyl; morpholinyl; piperidinyl; and piperazinyl, WO 01/16271 PCT/EPOO/08076 - 60 amine: the group -N(R) 2 , wherein each R is independently selected from: hydrogen; C1-C6-alkyl; and benzyl, halogen: selected from the group consisting of: F and Cl, 5 sulphonate: the group -S(0) 2 0R, wherein R is selected from: hydrogen; Cl-C6-alkyl; Na; K; Mg; and Ca, sulphate: the group -OS(0) 2 0R, wherein R is selected from: 10 hydrogen; Cl-C6-alkyl; Na; K; Mg; and Ca, sulphone: the group -S(0) 2 R, wherein R is selected from: hydrogen; C1-C6-alkyl; benzyl and amine selected from the group: -NR'2, wherein each R' is independently selected 15 from: hydrogen; Cl-C6-alkyl; and benzyl, carboxylate derivative: the group -C(O)OR, wherein R is selected from hydrogen; Na; K; Mg; Ca; Cl-C6-alkyl; and benzyl, 20 carbonyl derivative: the group: -C(O)R, wherein R is selected from: hydrogen; C1-C6-alkyl; benzyl and amine selected from the group: -NR'2, wherein each R' is independently selected from: hydrogen; Cl-C6-alkyl; and 25 benzyl, phosphonate: the group -P(O) (OR) 2 , wherein each R is independently selected from: hydrogen; C1-C6-alkyl, benzyl; Na; K; Mg; and Ca, 30 WO 01/16271 PCT/EPOO/08076 - 61 phosphate: the group -OP(O) (OR) 2 , wherein each R is independently selected from: hydrogen; C1-C6-alkyl; benzyl; Na; K; Mg; and Ca, 5 phosphine: the group -P(R) 2 , wherein each R is independently selected from: hydrogen; Cl-C6-alkyl; and benzyl, phosphine oxide: the group -P(O)R 2 , wherein R is 10 independently selected from: hydrogen; C1-C6-alkyl; benzyl and amine selected from the group: -NR'2, wherein each R' is independently selected from: hydrogen; Cl-C6-alkyl; and benzyl. 15 Other compounds or ligands forming complexes with transition metals, and which are capable of catalysing bleaching by atmospheric oxygen, are suitable as organic substances in the liquid bleaching compositions of the present invention. These include the classes of complexes of a transition metal 20 coordinated to a macropolycyclic ligand disclosed in WO-A 98/39098 and WO-A-98/39406. The liquid bleaching compositions according to the present invention may be used for laundry cleaning, hard surface 25 cleaning (including cleaning of lavatories, kitchen work surfaces, floors, mechanical ware washing etc.). As is generally known in the art, bleaching compositions are also employed in waste-water treatment, pulp bleaching during the manufacture of paper, leather manufacture, dye transfer 30 inhibition, food processing, starch bleaching, sterilisation, WO 01/16271 PCT/EPOO/08076 - 62 whitening in oral hygiene preparations and/or contact lens disinfection. In the context of the present invention bleaching should be 5 understood as relating generally to the decolourisation of stains or of other materials attached to or associated with a substrate. However, it is envisaged that the present invention can be applied where a requirement is the removal and/or neutralisation by an oxidative bleaching reaction of 10 malodours or other undesirable components attached to or otherwise associated with a substrate. Furthermore, in the context of the present invention bleaching is to be understood as being restricted to any bleaching mechanism or process that does not require the presence of light or activation by light. 15 Thus, photobleaching compositions and processes relying on the use of photobleach catalysts or photobleach activators and the presence of light are excluded from the present invention. In typical washing compositions the level of the organic 20 substance is such that the in-use level is from 0.05 yM to 50 mM, with preferred in-use levels for domestic laundry operations falling in the range 1 to 100 pM. Higher levels may be desired and applied in industrial bleaching processes, such as textile and paper pulp bleaching. 25 Preferably, the aqueous medium has a pH in the range from pH 6 to 13, more preferably from pH 6 to 11, and most preferably from 7 to 10. 30 The liquid bleaching composition of the present invention has particular application in detergent formulations, WO 01/16271 PCT/EPOO/08076 - 63 especially for laundry cleaning. Accordingly, in another preferred embodiment, the present invention provides a liquid detergent bleach composition comprising a liquid bleaching composition as defined above and additionally a 5 surface-active material, optionally together with detergency builder. In addition, the liquid bleaching composition may optionally contain soluble and non-soluble enzymes, enzyme stabiliser systems, functional polymers, polymers to modify the appearance and sensory properties of the liquid 10 bleaching composition and optionally other minors such as a perfume or a fluorescer. The liquid bleach composition according to the present invention may for example contain a surface-active material 15 in an amount of from 10 to 50% by weight. The surface active material may be naturally derived, such as soap, or a synthetic material selected from anionic, nonionic, amphoteric, zwitterionic, cationic actives and mixtures thereof. Many suitable actives are commercially available 20 and are fully described in the literature, for example in "Surface Active Agents and Detergents", Volumes I and II, by Schwartz, Perry and Berch. Typical synthetic anionic surface-actives are usually water 25 soluble alkali metal salts of organic sulphates and sulphonates having alkyl groups containing from about 8 to about 22 carbon atoms, the term "alkyl" being used to include the alkyl portion of higher aryl groups. Examples of suitable synthetic anionic detergent compounds are sodium 30 and ammonium alkyl sulphates, especially those obtained by sulphating higher (C 8

-C

18 ) alcohols produced, for example, WO 01/16271 PCT/EPOO/08076 - 64 from tallow or coconut oil; sodium and ammonium alkyl (C 9 C 2 0 ) benzene sulphonates, particularly sodium linear secondary alkyl (Cio-C 15 ) benzene sulphonates; sodium alkyl glyceryl ether sulphates, especially those ethers of the 5 higher alcohols derived from tallow or coconut oil fatty acid monoglyceride sulphates and sulphonates; sodium and ammonium salts of sulphuric acid esters of higher (C 9

-C

18 ) fatty alcohol alkylene oxide, particularly ethylene oxide, reaction products; the reaction products of fatty acids such 10 as coconut fatty acids esterified with isethionic acid and neutralised with sodium hydroxide; sodium and ammonium salts of fatty acid amides of methyl taurine; alkane monosulphonates such as those derived by reacting alpha olefins (C 8

-C

2 0 ) with sodium bisulphite and those derived by 15 reacting paraffins with SO 2 and Cl 2 and then hydrolysing with a base to produce a random sulphonate; sodium and ammonium

(C

7

-C

12 ) dialkyl sulphosuccinates; and olefin sulphonates, which term is used to describe material made by reacting olefins, particularly (Cio-C 2 0 ) alpha-olefins, with SO 3 and 20 then neutralising and hydrolysing the reaction product. The preferred anionic detergent compounds are sodium (C 10

-C

15 ) alkylbenzene sulphonates, and sodium (C 16

-C

18 ) alkyl ether sulphates. 25 Examples of suitable nonionic surface-active compounds which may be used, preferably together with the anionic surface active compounds, include, in particular, the reaction products of alkylene oxides, usually ethylene oxide, with alkyl (C 6

-C

22 ) phenols, generally 5-25 EO, i.e. 5-25 units of 30 ethylene oxides per molecule; and the condensation products of aliphatic (C 8

-C

18 ) primary or secondary linear or branched WO 01/16271 PCT/EPOO/08076 - 65 alcohols with ethylene oxide, generally 2-30 EO. Other so called nonionic surface-actives include alkyl polyglycosides, sugar esters, long-chain tertiary amine oxides, long-chain tertiary phosphine oxides and dialkyl 5 sulphoxides. The non-ionic surfactant liquid may be applied/ added in the form of a water-soluble sachet. Amphoteric or zwitterionic surface-active compounds can also be used in the compositions of the invention. If any 10 amphoteric or zwitterionic detergent compounds are used, it is generally in small amounts in compositions based on the much more commonly used synthetic anionic and nonionic actives. 15 The liquid detergent bleach composition of the invention may comprise from 1 to 40 % wt of anionic surfactant and from 0 to 40 % by weight of nonionic surfactant. The liquid detergent may contain any mixture of non-ionic, anionic, cationic zwitterionic or combination thereof. Optionally, 20 fatty acid soaps (0-30%) may be present. The liquid detergent bleach composition of the present invention may also contains a detergency builder, for example in an amount of from about 5 to 80 % by weight, preferably from about 10 to 60 % by weight. 25 Builder materials may be selected from 1) calcium sequestrant materials, 2) precipitating materials, 3) calcium ion-exchange materials and 4) mixtures thereof.

WO 01/16271 PCT/EP00/08076 - 66 Examples of calcium sequestrant builder materials include alkali metal polyphosphates, such as sodium tripolyphosphate; nitrilotriacetic acid and its water soluble salts; the alkali metal salts of carboxymethyloxy 5 succinic acid, ethylene diamine tetraacetic acid, oxydisuccinic acid, mellitic acid, benzene polycarboxylic acids, citric acid; and polyacetal carboxylates as disclosed in US-A-4,144,226 and US-A-4,146,495. 10 Examples of precipitating builder materials include sodium orthophosphate and sodium carbonate. Examples of calcium ion-exchange builder materials include the various types of water-insoluble crystalline or 15 amorphous aluminosilicates, of which zeolites are the best known representatives, e.g. zeolite A, zeolite B (also known as zeolite P), zeolite C, zeolite X, zeolite Y and also the zeolite P-type as described in EP-A-0,384,070. 20 In particular, the liquid bleaching compositions of the invention may contain any one of the organic and inorganic builder materials, though, for environmental reasons, phosphate builders are preferably omitted or only used in very small amounts. Typical builders usable in the present 25 invention are, for example, sodium carbonate, calcite/carbonate, the sodium salt of nitrilotriacetic acid, sodium citrate, carboxymethyloxy malonate, carboxymethyloxy succinate and water-insoluble crystalline or amorphous aluminosilicate builder materials, each of which can be used 30 as the main builder, either alone or in admixture with minor amounts of other builders or polymers as co-builder.

WO 01/16271 PCT/EPOO/08076 - 67 It is preferred that the liquid bleaching composition contains not more than 5% by weight of a carbonate builder, expressed as sodium carbonate, more preferably not more than 2.5 % by weight to substantially nil, if the composition pH 5 lies in the lower alkaline region of up to 10. Apart from the components already mentioned, the liquid bleaching composition of the present invention can contain any of the conventional additives in amounts of which such 10 materials are normally employed in fabric washing detergent compositions. Examples of these additives include buffers such as carbonates, lather boosters, such as alkanolamides, particularly the monoethanol amides derived from palmkernel fatty acids and coconut fatty acids; lather depressants, 15 such as alkyl phosphates and silicones; anti-redeposition agents, such as sodium carboxymethyl cellulose and alkyl or substituted alkyl cellulose ethers; stabilisers, such as phosphonic acid derivatives (i.e. Dequest® types); fabric softening agents; inorganic salts and alkaline buffering 20 agents, such as sodium sulphate and sodium silicate; and, usually in very small amounts, fluorescent agents; perfumes; enzymes, such as proteases, cellulases, lipases, amylases and oxidases; germicides and colourants. 25 Transition metal sequestrants such as EDTA, and phosphonic acid derivatives such as EDTMP (ethylene diamine tetra(methylene phosphonate)) may also be included, in addition to the organic substance specified, for example to improve the stability sensitive ingredients such as enzymes, 30 fluorescent agents and perfumes, but provided the composition remains bleaching effective. However, the WO 01/16271 PCT/EPOO/08076 - 68 liquid bleaching composition according to the present invention containing the organic substance, is preferably substantially, and more preferably completely, devoid of transition metal sequestrants (other than the organic 5 substance). Whilst the present invention is based on the catalytic bleaching of a substrate by atmospheric oxygen or air, it will be appreciated that small amounts of hydrogen peroxide 10 or peroxy-based or -generating systems may be included in the liquid composition, if desired, provided that the chemical and physical stability of the composition is not thereby adversely affected to an unacceptable level. Therefore, by "substantially devoid of peroxygen bleach or 15 peroxy-based or -generating bleach systems" is meant that the liquid bleaching composition contains from 0 to 50 %, preferably from 0 to 10 %, more preferably from 0 to 5 %, and optimally from 0 to 2 % by molar weight on an oxygen basis, of peroxygen bleach or peroxy-based or -generating 20 bleach systems. Preferably, however, the liquid bleaching composition will be wholly devoid of peroxygen bleach or peroxy-based or -generating bleach systems. Thus, at least 10 %, preferably at least 50 % and optimally at 25 least 90 % of any bleaching of the substrate is effected by oxygen sourced from the air. According to the fourth aspect, the organic substance in the liquid bleaching composition may be contacted to the textile 30 fabric in any suitable manner. For example, it may be applied in a liquor that is then dried, for example as an WO 01/16271 PCT/EP00/08076 - 69 aqueous spray-on fabric treatment fluid or a wash liquor for laundry cleaning, or a non-aqueous dry cleaning fluid or spray-on aerosol fluid. Other suitable means of contacting the organic substance in liquid form to the textile may be 5 used, as further explained below. Any suitable textile that is susceptible to bleaching or one that one might wish to subject to bleaching may be used. Preferably the textile is a laundry fabric or garment. 10 In a preferred embodiment of the fourth aspect, the method is carried out on a laundry fabric using an aqueous treatment liquor. In particular, the treatment may be effected in a wash cycle for cleaning laundry. More 15 preferably, the treatment is carried out in an aqueous detergent bleach wash liquid. In a preferred embodiment, the treated textile is dried, by allowing it to dry under ambient temperature or at elevated temperatures. 20 The bleaching method of the fourth aspect may be carried out by simply leaving the substrate in contact with the organic substance in the liquid bleaching composition for a sufficient period of time. Preferably, however, the organic substance is in an aqueous medium, and the aqueous medium on or containing 25 the substrate is agitated. In a preferred embodiment of the fourth aspect, the treated textile is dried, by allowing it to dry under ambient temperature or at elevated temperatures. 30 WO 01/16271 PCT/EPOO/08076 - 70 In a particularly preferred embodiment the method according to the fourth aspect is carried out on a laundry fabric using aqueous treatment liquor. In particular the treatment may be effected in, or as an adjunct to, an essentially 5 conventional wash cycle for cleaning laundry. More preferably, the treatment is carried out in an aqueous detergent wash liquor. Preferably, the organic substance is delivered into the wash liquor from a liquid concentrate. 10 It is particularly advantageous that the organic substance in liquid composition used in the method of the fourth aspect makes use of atmospheric oxygen in its bleaching activity. This avoids the requirement that peroxygen bleaches and/or other relatively large quantities of 15 reactive substances need be used in the treatment process. Consequently, only a relatively small quantity of bleach active substance in liquid composition need be employed and this allows dosage routes to be exploited, which could previously not be used. Thus, while it is preferable to 20 include the organic substance in a liquid composition that is normally used in a washing process, such as a pre treatment, main-wash, conditioning composition or ironing aid, other means for ensuring that the organic substance is present in the wash liquor may be envisaged. 25 For example, it is envisaged that the organic substance in the liquid composition can be presented in the form of a body from which it is slowly released during the whole or part of the laundry process. Such release can occur over the 30 course of a single wash or over the course of a plurality of washes. In the latter case it is envisaged that the organic WO 01/16271 PCT/EPOO/08076 - 71 substance in liquid composition can be released from a carrier substrate used in association with the wash process, e.g. from a body placed in the dispenser drawer of a washing machine, elsewhere in the delivery system or in the drum of 5 the washing machine. When used in the drum of the washing machine the carrier can be freely moving or fixed relative to the drum. Such fixing can be achieved by mechanical means, for example by barbs that interact with the drum wall, or employ other forces, for example a magnetic force. 10 The modification of a washing machine to provide for means to hold and retain such a carrier is envisaged similar means being known from the analogous art of toilet block manufacture. Freely moving carriers such as shuttles for dosage of surfactant materials and/or other detergent 15 ingredients into the wash can comprise means for the release of the organic substance in the liquid composition into the wash. In the alternative, the organic substance can be presented 20 in the form of a liquid wash additive that preferably is soluble. Dosage of the additive can be unitary or in a quantity determined by the user. While it is envisaged that such additives can be used in the main washing cycle, the use of them in the conditioning or drying cycle is not 25 hereby excluded. The present invention is not limited to those circumstances in which a washing machine is employed, but can be applied where washing is performed in some alternative vessel. In 30 these circumstances it is envisaged that the organic substance in liquid composition can be delivered by means of WO 01/16271 PCT/EPOO/08076 - 72 slow release from the bowl, bucket or other vessel which is being employed, or from any implement which is being employed, such as a brush, bat or dolly, or from any suitable applicator for liquid compositions. 5 Suitable pre-treatment means for application of the organic substance from the liquid composition to the textile material prior to the main wash include sprays, pens, roller-ball devices and impregnated cloths or cloths 10 containing microcapsules. Such means are well known in the analogous art of deodorant application and/or in spot treatment of textiles. Similar means for application are employed in those embodiments where the organic substance in liquid composition is applied after the main washing and/or 15 conditioning steps have been performed, e.g. prior to or after ironing or drying of the cloth. For example, the organic substance in liquid composition may be applied using tapes, sheets or sticking plasters coated or impregnated with the substance, or containing microcapsules of the 20 substance. The organic substance in liquid composition may for example be incorporated into a drier sheet so as to be activated or released during a tumble-drier cycle, or the organic substance in liquid composition can be provided in an impregnated or microcapsule-containing sheet so as to be 25 delivered to the textile when ironed. The invention will now be further illustrated by way of the following non-limiting examples: WO 01/16271 PCT/EPOO/08076 - 73 EXAMPLES Example 1 5 This example describes a synthesis of the catalyst as employed in Example 2: (i) Preparation of MeN4Py ligand: N,N-bis(pyridin-2-yl-methyl)-1,1-bis(pyridin-2-yl)-1 10 aminoethane, MeN4Py, was prepared according to the procedure found in EP 0 909 809 A. (ii) Synthesis of the complex FeMeN4PyCl 2 : MeN4Py ligand (33.7 g; 88.5mmoles) was dissolved in 500ml 15 dry methanol. Small portions of FeCl 2 .4H 2 0 (0.95eq; 16.7g; 84.Ommoles) were added, yielding a clear red solution. After addition, the solution was stirred for 30 minutes at room temperature, after which the methanol was removed (rotary evaporator). The dry solid was ground and 150 ml of 20 ethylacetate was added and the mixture was stirred until a fine red powder was obtained. This powder was washed twice with ethyl acetate, dried in the air and further dried under vacuum (40 oC). El. Anal. Calc. for [Fe(MeN4py)Cl]Cl.2H 2 0: C 53.03; H 5.16; N 12.89; Cl 13.07; Fe 10.01%. Found C 52.29/ 25 52.03; H 5.05/5.03; N 12.55/12.61; Cl: 12.73/12.69; Fe: 10.06/10.01%. Example 2: 30 Experiments with the FeMeN4PyCl 2 complex in a variety of liquid detergents were performed to establish bleaching WO 01/16271 PCT/EP00/08076 - 74 activity in various liquid detergent formulations and to determine stability upon storage. FeMeN4PyCl 2 complex was added to several liquid detergent 5 products and the stability and activity observed during storage. The following commercially available liquid detergent compositions were used as base liquids: a) WISKTM liquid USA, 10 1999; b) OMOTM liquid NL, 1999; c) OMO-liquido TM Brazil, 1999; and d) Rinse conditioner (Robijn TM - NL). Incorporation of FeMeN4PyCl 2 in liquid detergents: FeMeN4PyCl 2 was incorporated by post dosing a stock solution 15 of 0.01 g/ml using an electrical stirrer (125 rpm, Heidolph RZR 2101). The final concentration in the product was 0.1% for all products. To the reference a same amount of water was added by post dosing to compensate for the post dose volume of the stock solution. 20 The activity of FeMeN4PyCl 2 was measured by washing tomato oil (TO) cloth samples in mini bottles for 15 minutes at a temperature of 25 *C and a dosage of 2 g/l product at 10 OFH. All of the liquids prepared were initially stable and 25 homogeneous. The following table lists compositions prepared. As detailed above base liquids a) to d) have had FeMeN4PyC1 2 incorporated therein. Compositions 5 to 8 are control 30 liquids without added FeMeN4PyCl 2

.

WO 01/16271 PCT/EPOO/08076 - 75 Composition No. Liquids 1 WiskTM liquid USA, 1999 2 OMOTM liquid NL, 1999 3 OMO-liquido TM Brazil, 1999 4 Rinse conditioner (Robijn TM - NL) Reference Liquids 5 WiskTM liquid USA, 1999 6 OMOTM liquid NL, 1999 7 OMOTM -liquido T M Brazil, 1999 8 Rinse conditioner (Robijn TM - NL) Cloth samples were washed in mini bottles with a liquid:cloth ratio of 1:20 and the samples were dried in a 5 tumble dryer. Bleaching activity was measured directly after the wash (after 2 hours), and after 1 one-day (24 hours) storage in the dark in order to establish post wash bleach effects. The five 10 liquid formulations were stored under ambient conditions and the cleaning activity of the formulations without and with FeMeN4PyCl 2 was determined after certain periods of times. The times were immediately after preparation, and after 1, 2, 3, 4 and 6 weeks of storage. After the wash, the cloths were dried 15 in a tumble drier and the reflectance was measured with a MinoltaTM 3700d spectrophotometer at 460 nm. The difference in reflectance before and after the wash is defined as a AR460 value. 20 Tabulated results are shown in Tables 1 to 6 below.

WO 01/16271 PCT/EPOO/08076 - 76 Table 1 Directly after preparation TO-stain AR 460 TO-stain AR 460 10 FH, 2 g/l, T=25 C 2 hours after 1 day after washing washing Triplicate measurements average stdv average Stdv Composition 5 14.3 1.6 26.6 3.1 Composition 1 16.5 1.4 34.6 0.6 Composition 6 12.9 0.7 20.0 2.9 Composition 2 17.2 1.4 35.7 0.8 Composition 7 16.2 0.6 24.4 5.2 Composition 3 23.8 1.6 37.1 1.0 Composition 8 4.8 1.1 6.6 0.8 Composition 4 5.9 0.9 15.5 1.0 5 Table 2 1 week after preparation TO-stain AR 460 TO-stain AR 460 10 FH, 2 g/l, T=25 C 2 hours after 1 day after washing washing ___ Triplicate measurements average stdv average Stdv Composition 5 11.8 1.3 13.1 Composition 1 18.5 0.7 36.6 Composition 6 11.2 0.4 12.8 Composition 2 14.9 0.4 37.4 Composition 7 13.6 0.4 18.9 Composition 3 19.9 2.7 39.3 Composition 8 4.1 1.0 5.5 Composition 4 3.7 0.8 12.6 WO 01/16271 PCT/EPOO/08076 - 77 Table 3 2 weeks after preparation TO-stain AR 460 TO-stain AR 460 10 *FH, 2 g/l, T=25 C 2 hours after 1 day after washing washing Triplicate measurements average stdv average Stdv Composition 5 11.7 1.4 16.5 1.3 Composition 1 20.2 0.9 34.0 0.8 Composition 6 12.1 0.3 16.2 3.3 Composition 2 14.8 0.1 34.5 0.7 Composition 7 14.7 0.1 17.6 1.5 Composition 3 19.7 2.4 35.2 1.3 Composition 8 3.9 0.8 5.4 0.7 Composition 4 4.1 0.3 11.4 0.8 5 Table 4 3 weeks after preparation TO-stain AR 460 TO-stain AR ___ ___ ___ ___ __460 10 OFH, 2 g/l, T=-25 C 2 hours after 1 day after washing washing Triplicate measurements average stdv average Stdv Composition 5 13.5 0.6 16.9 2.5 ,Composition 1 14.1 1.7 33.8 1.0 Composition 6 12.8 0.5 17.6 3.2 Composition 2 14.5 0.5 34.1 1.4 Composition 7 16.1 1.8 18.8 4.5 Composition 3 16.6 0.9 33.9 0.3 Composition 8 3.1 0.7 4.2 1.6 Composition 4 3.9 0.8 7.8 1.2 WO 01/16271 PCT/EPOO/08076 - 78 Table 5 4 weeks after preparation TO-stain AR 460 TO-stain AR 460 10 *FH, 2 g/l, T=25 *C 2 hours after 1 day after washing washing Triplicate measurements average stdv average Stdv Composition 5 12.1 1.1 15.0 2.2 Composition 1 17.8 1.7 34.5 1.2 Composition 6 12.3 0.8 15.2 1.9 Composition 2 16.5 1.7 34.2 1.5 Composition 7 14.1 1.9 16.7 1.6 Composition 3 14.5 0.1 28.3 1.3 Composition 8 3.5 0.6 5.0 1.0 Composition 4 3.4 2.1 9.5 1.9 5 Table 6 6 weeks after preparation TO-stain AR 460 TO-stain AR 460 10 OFH, 2 g/l, T=25 0 C 2 hours after 1 day after washing washing Triplicate measurements average stdv average Stdv Composition 5 14.8 0.9 15.8 1.5 Composition 1 18.7 1.6 34.3 1.4 Composition 6 15.2 1.0 15.5 1.3 Composition 2 16.8 0.7 31.0 1.4 Composition 7 19.1 0.7 19.8 1.5 Composition 3 16.9 0.7 17.1 0.6 Composition 8 6.2 0.7 7.1 0.5 Composition 4 6.1 0.3 7.3 0.5 Example 3 10 Composition 5 WiskTM liquid USA, 1999 Composition 6 OMOTM liquid NL, 1999 Composition 7 OMO-liquido

TM

Brazil, 1999 WO 01/16271 PCT/EPOO/08076 - 79 Composition 9 non-aqueous liquid formulation: Ingredient Wt% Nonionic surfactant 26.6 Monopropylene glycol 5.5 Pigment premix 0.017 Glycerol 21.36 Monoethanolamine 7.56 Oleic fatty acid 13.10 Water Up to 100 Linear alkyl benzene 20.1 sulfonate Perfume 1.6 Protease Enzyme 1.0 In all experiments, 2 g/l of the above formulation was used, 5 with either 2.5 or 5 microM of metal complex 1-8, or 2.5 or 5 microM of the ligand 1-8 dissolved in the wash liquor. In all cases tomato stains were used and treated further as described for Example 3. The cloths were measured immediately after drying and after 24 h storage (expressed 10 as AR 460 bleaching value (a higher value indicates a cleaner cloth). Ligand 1: N,N-bis(pyridin-2-yl-methyl)-1,1-bis(pyridin-2 yl)-1-aminoethane (MeN4py). 15 Ligand 2: N,N-bis(pyridin-2-yl-methyl)-1,1-bis(pyridin-2 yl)-1-amino-2-phenylethane (BzN4py). The synthesis of ligand 2 has been disclosed in EP 0909 809.

WO 01/16271 PCT/EPOO/08076 - 80 Ligand 3: N,N-bis(pyridin-2-yl-methyl)-1,1-bis(pyridin-2 yl)-aminomethane (N4py). The synthesis of ligand 3 has been disclosed in Wo-A-9534628. 5 Ligand 4: N,N,N',N'-tetrakis(pyridin-2ylmethyl)ethane diamine (tpen). Ligand 4 was synthesised according to a modified literature procedure (see G. Anderegg, F. Wenk, Helv. Chim. Acta, 50(8), 2330 (1967). 10 Trispicen-NH (5.95 g, 17.9 mmol) and 1.67 g (18.4 mmol) of 2-pyridinecarboxaldehyde were dissolved in 120 ml 1,2 dichloroethane. To this mixture NaBH(OAc) 3 (18 mmol) was added and the mixture was refluxed for 16 h. Subsequently 50 ml of 5 N NaOH and after 1 h stirring the organic layer 15 was separated and the water layer was further extracted with dichloromethane. After drying the organic layers over sodium sulfate, filtration and evaporation of the solvents, a semi solid paste was obtained that was purified over an alumina column (elutant: ethyl acetate/ hexane/ triethylamine 20 9:10:1). The oil isolated become now solid and could be crystallised from ethyl acetate/hexane (1/1) yielding a pale-brown powder (4.45 g, 10.5 mmol; 58.6%). 1 H-nmr (CDCl 3 ) 8 2.78 (s, 4H); 3.75 (s, 8H); 7.0 (m, 4H); 7.38 (m, 4H); 7.50 (m, 4H) ; 8.43 (m, 4H). 25 Ligand 5: N-methyl-N,N',N'-tris(3-methyl-pyridin 2ylmethyl)ethane-diamine (trilen). The synthesis of ligand 5 has been disclosed in EP 1001 009. 30 Ligand 6: N,N,N'-tris(pyridin-2ylmethyl)ethane-diamine (trispicen-NH).

WO 01/16271 PCT/EPOO/08076 - 81 First N,N'-bis(pyridin-2ylmethyl)-ethanediamine (bispicen) was synthesised by the following procedure. Ethylenediamine (26 ml, 0.38 mol) was dissolved in 200 ml dry methanol. To this mixture 74 ml (0.76 mol) pyridincarboxaldehyde was 5 added. The mixture was refluxed for 2 h, after which the mixture was left to cool to RT and in small portions 40 g of NaBH 4 was added. The mixture was subsequently stirred for 16 h at RT. The methanol was evaporated and 500 ml of water was added. The aqueous mixture was extracted by three portions 10 of dichloromethane (100 ml) and the dichloromethane solution was dried over sodium sulfate, filtered off and the solvent was removed. The dark oil containing N,N'-bis(pyridin 2ylmethyl)-ethanediamine (73.7 g; 81%) was analysed by NMR and used without further purification. 'H-nmr (CDCl 3 ) : 2.20 15 (br, NH); 2.78 (s, 4H); 3.85 (s, 4H); 7.00-7,7.40 (m, 4H); 7.58 (m, 2H); 8.45 (m, 2H). In the second step the aminal of bispicen with 2 pyridincarboxaldehyde was synthesised. 73,7 g of the 20 unpurified bispicen material (see above) was under argon dissolved in 750 ml of dry diethyether (distilled over P 2 0 5 . To this solution 32.8 of 2-pyridincarboxaldehyde was added, the reaction mixture was stirred and cooled in an ice/water bath. After 20 min a white precipitate was formed that was 25 filtered off (P4-glass filter) and dried with dry ether. The yield was 66.6 g (66%) and was used without further purification. 'H-nmr (CDCl 3 ) : 2.75 (m, 2H) ; 3.13 (m, 2H) 3.65 (d, 2H); 4.93 (d, 2H); 4.23 (s, 1H); 7.00-7.90 (m, 9H); 8.43 (m, 3H). 30 WO 01/16271 PCT/EPOO/08076 - 82 In the third step the desired ligand was obtained (N,N,N' tris(pyridin-2ylmethyl)ethane-diamine - trispicen-NH). The aminal (45.0 g; 0.135 mol), obtained as described as above, was dissolved in 1.2 1 of dry methanol (distilled over Mg), 5 and to this mixture 8.61 g (0.137 mol) of NaBCNH 3 was added in small portions. Subsequently 21 ml of trifluoroacetic acid was added dropwise in the solution. The mixture was stirred for 16 h at RT and subsequently 1.05 L of SN NaOH was added and the mixture was stirred for 6 h. Extraction 10 with dichloromethane yielded after drying, filtration and removal of the solvent a yellow oil as product (42.7 g , 0.128 mol; 95%. 1 H-nmr (CDC1 3 ): 8 2.15 (br, NH) ; 2.75 (s, 4H); 3.80 (s, 4H); 3.82(s, 2H); 7.0-7.8 (m, 3H); 7.45-7.70 (m, 6H); 8.40-8.60 (m, 3H). 13 C-nmr (CDCl 3 ) 8 53.9 (t) ; 54.7 15 (t); 60.4 (t); 121.7 (d); 121.9 (d); 122.1 (d); 123.0 (d); 136.3 (d); 136.4 (d); 148.9 (d); 149.1 (d); 159.3 (s); 159.6 (s). Ligand 7: N-methyl-,N,N'N'-tris(pyridin-2ylmethyl)ethane 20 diamine (trispicen-NMe). Ligand 7 was prepared according to a modified procedure described by Bernal et al (J. Chem. Soc., Dalton Trans, 22, 3667 (1995)). Trispicen-NH (log, 30 mmol) was dissolved in 25 ml formic acid and 10 ml water. To this mixture 36 % formaldehyde 25 solution was added (16 ml, 90 mmol) and the mixture was warmed up till 90 OC for 3 h. Formic acid was evaporated and the 2.5 N NaOH solution was added until the pH was higher than 9. Extraction by dichloromethane and drying over sodium sulfate, filtration of the solution and subsequently drying 30 yielded a dark-coloured oil (8.85g). The oil was purified over a alumina column (elutant: ethyl acetate/ hexane/ WO 01/16271 PCT/EPOO/08076 - 83 triethylamine 9:10:1). Yield 7,05g pale yellow oil (20,3mmoles; 68%) . 'H-nmr (CDCl 3 ) : 2.18 (s, 3H) ; 2.65 (m, 2H); 2.75 (m, 2H); 3.60 (s; 2H); 3.83 (s; 4H); 7.10 (m, 3H); 7.3-7.6 (m, 6H); 8.5 (d, 3H). 5 Ligand 8: tris(pyridin-2-ylmethyl)amine (tpa) Ligand 8 was prepared according to literature procedures (see G. Anderegg, F. Wenk,, Helv. Chim. Acta, 50(8), 2330 (1967). 10 Complex 1: [(MeN4Py)FeCl]C1 The synthesis of Complex 1 is described in Example 1. Complex 2: [(BzN4Py)Fe(CH 3 CN)] (C104) 2 15 The synthesis of Complex 2 is described in EP 0909 809. An optimised synthetic procedure is given below: 3.0 g (6.56 mmol) of BzN4Py was dissolved in 30ml methanol and 30ml acetonitrile. 2.26 g (6.23 mmol) of Fe(C10 4 ) .6H 2 0 (Aldrich) was added to solution containing the ligand in small 20 portions. To the dark-red coloured solution in total 100 ml of ethyl acetate was added to facilitate the crystallisation procedure. After 18 h stirring, the red powder was filtered off, washed with ethyl acetate and dried, yielding 3.85 g of the desired complex (anal: see EP 0909 809). 25 Complex 3: [(N4Py)FeC1C1 Complex 3 was synthesised according to the procedure as described for the analogous MeN4py complex using now N4py as ligand (see example 1). 30 Complex 4: [(tpen)Fe] (C0 4

)

2 WO 01/16271 PCT/EPOO/08076 - 84 Complex 4 was prepared according to the procedure found in H. Toftlund et al., J.Am. Chem. Soc., 112, 6814 (1990) Complex 5: [(trilen)FeCl]PF 6 5 Complex 5 was prepared according to EP 1001 009 Complex 6: [(trispicen-NH)FeC1PF 6 Trispicen-NH (8.0 g; 24.0 mmol) was dissolved in 60 ml methanol/water 1/1 v/v) and was heated till 50 *C. FeC1 2 .4H 2 0 10 4,78g; 24,ommoles)was added in small portions. The dark blue-purple solution was stirred for 10 min at 50 *C. Subsequently 4.42 g (24 mmol) of KPF 6 was added and the solution was stirred for 2 days at RT. The dark powder was filtered, washed with methanol/water and then with ethyl 15 acetate. The powder was dried in the air. Yield 11.6 g. Complex 7: [(trispicen-NMe)FeCl]PF 6 TrispicenNMe (6,0g; 17,3mmoles) was dissolved in 15 ml methanol/water 1/1 v/v) and was heated till 50 *C. FeCl 2 .4H 2 0 20 3,43g; 17,Ommoles), dissolved in 20 ml water/methanol 1/1), was added. The dark solution was stirred for 20 min at 50 *C. Subsequently 3.17 g (17 mmol) of KPF 6 dissolved in 10 ml water, was added and the solution was stirred for 15 h to yield a yellow precipitation. The solid was filtered off, 25 wasged with methanol/water 1/1, v/v) and ethyl acetate. Drying yielded 8.25 g of a pale-yellow powder. Complex 8: [Fe 2 (tpa) 2

(H

2 0)2] (C104) 2 Complex 8 was kindly donated by Prof. L. Que, University of 30 Minnesota, USA (references: L. Que et al., Inorg Chim. Acta, WO 01/16271 PCT/EPOO/08076 - 85 273, 393 (1998) and H. Toftlund et al., Inorg. Chem., 33, 3127 (1994). Table 7. Bleaching results obtained on tomato stains for the 5 different complexes (5 microM) in solutions containing the four liquid formulations (compositions 5, 6, 7 and 9). The bleaching results obtained immediately after drying (t=0) and after 1 day storage are shown. All values expressed in AR 460 values; typical errors are in the order of 2 points. 10 Comp 5 Comp 6 Comp 7 Comp 9 t=0 t=1 t=0 t=1 t=0 t=1 t=0 t=1 Complex 1 20 50 41 47 35 55 42 49 Complex 2 20 48 42 50 31 51 42 52 Complex 3 31 49 35 50 31 53 44 52 Complex 4 16 39 16 23 26 48 29 42 Complex 5 33 47 36 46 39 52 43 50 Complex 6 15 22 12 15 16 23 15 18 Complex 7 19 39 17 20 25 46 27 33 Blank 11 13 15 19 13 14 15 18 From these results is clear that especially complexes 1, 2, 3, and 5 give a good tomato stain bleaching with air, 15 although the exact amount depends on the formulation employed. Complexes 4, 6, and 7 give somewhat lower bleaching activity, but still in most cases more than the blanks.

WO 01/16271 PCT/EPOO/08076 - 86 Table 8. Bleaching results obtained on tomato stains for the different ligands (5 microM) in solutions containing the four liquid formulations (compositions 5, 6, 7 and 9). The 5 bleaching results obtained immediately after drying (t=0) and after 1 day storage are shown. All values expressed in AR 460 values; typical errors are in the order of 2 points. Comp 5 Comp 6 Comp 7 Comp 9 t=O t=1 t=0 t=1 t=0 t=1 t=0 t=1 Ligand 1 16 42 22 44 18 32 33 52 Ligand 2 16 40 26 47 16 34 32 51 Ligand 3 18 37 19 39 18 39 33 53 Ligand 5 22 40 26 36 19 36 41 52 Ligand 6 14 16 14 16 14 20 18 20 Ligand 7 16 20 16 19 19 28 19 22 Blank 11 13 14 19 12 14 15 18 10 All ligands in the wash liquor containing the four formulations give significant enhancement of the tomato stain bleaching in the air. This effect is especially clear for ligands 1, 2, 3 and 5. 15 Table 9. Bleaching results obtained on tomato stains for the different complexes (2.5 microM) in solutions containing the four liquid formulations (compositions 5, 6, 7 and 9). The bleaching results obtained immediately after drying (t=0) 20 and after 1 day storage are shown. All values expressed in AR 460 values; typical errors are in the order of 2 points.

WO 01/16271 PCT/EPOO/08076 - 87 Comp 5 Comp 6 Comp 7 Comp 9 t=0 t=1 t=0 t=1 t=0 t=1 t=0 t=1 Complex 1 15 46 38 48 27 49 22 44 Complex 2 22 46 15 35 28 47 18 38 Complex 3 20 46 24 43 27 44 24 47 Complex 4 12 19 9 11 18 24 12 19 Complex 5 30 43 23 33 27 36 23 40 Complex 6 9 10 8 9 16 23 13 14 Complex 7 15 18 9 10 23 32 17 21 Complex 8 10 13 11 12 11 13 12 15 Blank 10 11 9 10 12 14 11 12 Table 10. Bleaching results obtained on tomato stains for the different ligands (2.5 microM) in solutions containing the four liquid formulations (compositions 5, 6, 7 and 9). 5 The bleaching results obtained immediately after drying (t=0) and after 1 day storage are shown. All values expressed in AR 460 values; typical errors are in the order of 2 points. Comp 5 Comp 6 Comp 7 Comp 9 t=0 t=1 t=0 t=1 t=0 t=1 t=0 t=1 Ligand 1 13 26 9 13 11 13 11 15 Ligand 2 11 19 10 14 10 13 13 21 Ligand 3 13 26 9 11 12 14 13 17 Ligand 5 13 20 9 11 12 16 14 19 Ligand 6 11 12 10 12 10 11 10 12 Ligand 7 12 15 9 11 10 12 13 15 Ligand 8 8 9 9 11 13 15 11 14 Blank 10 11 9 10 11 14 11 12 WO 01/16271 PCT/EPOO/08076 - 88 Discussion of Results: The results show that the activity of FeMeN4PyC1 2 is stable for six weeks in the detergent Compositions 1 and 2. However, the activity of FeMeN4PyCl 2 in composition 4 and in 5 composition 3 after more than four weeks storage decreased. Without being bound by theory, it is more than likely that STP present in a liquid composition gives the negative effect on the storage stability and that addition of iron salt restores the activity. The results show that by adding 10 a liquid composition containing a ligand or transition metal complex thereof to the wash liquor a bleaching capacity is provided without the presence of an added peroxyl species or precursor thereof. In addition, the bleaching capacity is provided at a low concentration of a ligand or transition 15 metal complex thereof in the wash liquor. 1) FeMeN4PyCl 2 , amongst others, gives clear bleach benefits in a variety of liquid formulations (incl. rinse conditioner) on tomato-oil stains. 20 2) The bleach effect upon 24 hr storage of the cloths in the dark is much larger then 2 h after the wash. 3) No visual change in structural phase after two weeks. 4) Immediate colour change upon addition of FeMeN4PyCl 2 of the liquid observed. 25 5) Similar bleach performance upon 6 weeks of storage as found immediately after mixing for the detergent Compositions 1 and 2, implying a stable system. 6) No bleach effects were more observed after 6 weeks of storage for detergent Composition 3 and rinse conditioner 30 Composition 4.

WO 01/16271 PCT/EPOO/08076 - 89 Complex 8 and ligand 8 show significant decreased bleach benefit in a liquid bleach composition. As is known from inorganic chemistry, in general pentadentate ligands give rise to more stable complexes than tetradenate ligands; this 5 is known as the chelate effect. (see Huheey, inorganic chemistry, 2 d edition, Harper and Row). The decreased stability is especially noted in basic aqueous media, where formation of insoluble iron Hydroxide species are often encountered. The decreased stability of the iron tpa 10 complexes/species gives rise to a poorer performance in the liquid detergent formulations. There are many liquid formulations for detergents and rinse conditioners or other liquid products that may be enhanced 15 by conferring a bleaching ability to the liquid formulation. As will be evident to one skilled in the art the present invention is applicable to known liquid formulations and liquid formulations to be developed. 20 As one skilled in the art will appreciate determining the suitability of a particular catalyst for bleaching of a substrate by atmospheric oxygen in a particular liquid formulation is a matter of routine experimentation. The present invention extends to both isotropic and complex 25 liquid compositions and formulations a brief discussion of which follows. Some isotropic formulations are termed 'micro-emulsion' liquids that are clear and thermodynamically stable over a specified temperature range. The 'micro-emulsion' formulation may be water in oil, or oil 30 in water emulsions. Some liquid formulations are macro emulsions that are not clear and isotropic. Emulsions are WO 01/16271 PCT/EPOO/08076 - 90 considered meta-stable. Concentrated, clear compositions containing fabric softening actives have been disclosed in WO 98/08924 and WO 98/4799, both Procter & Gamble. Such compositions comprise bio-degradable fabric conditioners. 5 However, both disclose compositions comprising water miscible solvents that do not form water-in-oil micro emulsions. Clear fabric conditioning compositions have also been disclosed in EP 730023 (Colgate Palmolive), WO 96/19552 (Colgate Palmolive), WO 96/33800 (Witco Co.), WO 97/03170 10 (Procter & Gamble), WO 97/03172 (Procter & Gamble), WO 97/03169 (Procter & Gamble), US 5492636 (Quest Int.) and US 5427697 (Procter & Gamble). Liquid formulations of the present invention may contain for example; monoethoxy quats; AQAs and bis-AQAs; cationic amides; cationic esters; 15 amino/diamino quats; glucamide; amine oxides; ethoxylated polyethyleneimines; enhancement polymers of the form linear amine based polymers, e.g. bis-hexamethylenetriamine; polyamines e.g. TETA, TEPA or PEI polymers. 20 Experimentation to determine catalyst-liquid stability, as detailed above, may be varied. The aforementioned method determined the catalyst-liquid stability/compatibility by examining how the oxygen bleaching ability of a particular catalyst-liquid formulation varied with time. 25 Alternatively, the determination may be conducted by monitoring the concentration of a particular catalyst in a liquid formulation by known techniques, for example NMR, HPLC, Liquid Chromatography-Mass Spectroscopy, Infra Red, U V-visible measurements, etc, over a period of time. 30 Alternatively, another possible method of determining catalyst-liquid stability would be to analyse the activity WO 01/16271 PCT/EPOO/08076 - 91 of a certain transition metal compound by oxidation activity studies using a dye/compound that gives a colour change upon oxidation. An example of a dye/compound that gives a colour change upon oxidation is 2,2'-azinobis(3 5 ethylbenzothiazoline-6-sulfonate) and many other dyes/compounds that give a colour change upon oxidation are known. Methods for using a dye/compound that gives a colour change upon oxidation are known in the art for establishing activity of a variety of redox enzymes. 10

Claims (12)

1. A liquid bleaching composition comprising an organic substance which forms a complex with a transition metal, the 5 complex catalysing bleaching of a substrate by atmospheric oxygen, and a liquid carrier or solvent, wherein the composition is substantially devoid of peroxygen bleach or a peroxy-based or -generating bleach system. 10 2. A liquid bleaching composition according to claim 1, wherein the organic substance comprises a pentadentate ligand of the general formula (B): R1 12 R 3 -C N R 1 R 2 15 (B) wherein each R 1 , R 2 independently represents -R 4 -Rs R 3 represents hydrogen, optionally substituted alkyl, aryl or arylalkyl, or -R4-Rs, 20 each R 4 independently represents a single bond or optionally substituted alkylene, alkenylene, oxyalkylene, aminoalkylene, alkylene ether, carboxylic ester or carboxylic amide, and each R5 independently represents an optionally N 25 substituted aminoalkyl group or an optionally substituted heteroaryl group selected from pyridinyl, pyrazinyl, WO 01/16271 PCT/EPOO/08076 - 93 pyrazolyl, pyrrolyl, imidazolyl, benzimidazolyl, pyrimidinyl, triazolyl and thiazolyl.

3. A liquid bleaching composition according to claim 2, 5 wherein the ligand is N,N-bis(pyridin-2-yl-methyl)-1,1 bis(pyridin-2-yl)-1-aminoethane.

4. A liquid bleaching composition according to any of claims 1 to 3, wherein the medium has a pH value in the 10 range from pH 6 to 11.

5. A liquid bleaching composition according to claim 4, wherein the medium has a pH value in the range from pH 7 to

10. 15 6. A liquid bleaching composition according to any of claims 1 to 5, wherein the medium is substantially devoid of a transition metal sequestrant. 20 7. A liquid bleaching composition according to any of claims 1 to 6, wherein the medium further comprises a surfactant. 8. A liquid bleaching composition according to any of 25 claims 1 to 7, wherein the medium further comprises a builder. 9. A liquid bleaching composition according to any of claims 1 to 8, wherein the organic substance comprises a 30 preformed complex of a ligand and a transition metal. WO 01/16271 PCT/EPOO/08076 - 94 10. A liquid bleaching composition according to any of claims 1 to 8, wherein the organic substance comprises a free ligand that complexes with a transition metal present in the water. 5

11. A liquid bleaching composition according to any of claims 1 to 8, wherein the organic substance comprises a free ligand that complexes with a transition metal present in the substrate. 10

12. A liquid bleaching composition according to any of claims 1 to 8, wherein the organic substance comprises a composition of a free ligand or a transition metal substitutable metal-ligand complex, and a source of 15 transition metal.

13. A method of bleaching a substrate comprising applying to the substrate a liquid bleaching composition that comprises an organic substance which forms a complex with a 20 transition metal, the complex catalysing bleaching of the substrate by atmospheric oxygen, and a liquid carrier or solvent, wherein the composition is substantially devoid of peroxygen bleach or a peroxy-based or -generating bleach system. 25

14. A method to claim 13, wherein the organic substance comprises a pentadentate ligand of the general formula (B): WO 01/16271 PCT/EPOO/08076 - 95 R1 P2 R3-C N RI R 2 (B) wherein 5 each R 1 , R 2 independently represents -R 4 -Rs, R 3 represents hydrogen, optionally substituted alkyl, aryl or arylalkyl, or -R-R', each R 4 independently represents a single bond or optionally substituted alkylene, alkenylene, oxyalkylene, 10 aminoalkylene, alkylene ether, carboxylic ester or carboxylic amide, and each R 5 independently represents an optionally N substituted aminoalkyl group or an optionally substituted heteroaryl group selected from pyridinyl, pyrazinyl, 15 pyrazolyl, pyrrolyl, imidazolyl, benzimidazolyl, pyrimidinyl, triazolyl and thiazolyl.

15. A method according to claim 14, wherein the ligand is N,N-bis (pyridin-2-yl-methyl) -1, 1-bis (pyridin-2-yl) -1 20 aminoethane.

16. A method according to any of claims 13 to 15, wherein the medium is as defined in any of claims 4 to 8. 25 17. Use of an organic substance which forms a complex with a transition metal, the complex catalysing bleaching of a substrate by the atmospheric oxygen, as a catalytic WO 01/16271 PCT/EPOO/08076 - 96 bleaching agent in a liquid bleaching composition substantially devoid of peroxygen bleach or a peroxy-based or -generating bleach system. 5 18. A method of treating a textile by contacting the textile with a liquid bleaching composition that comprises an organic substance which forms a complex with a transition metal, the complex catalysing bleaching by atmospheric oxygen, and a liquid carrier or solvent, wherein the 10 composition is substantially devoid of peroxygen bleach or a peroxy-based or -generating bleach system, whereby the complex catalyses bleaching of the textile by atmospheric oxygen after the treatment. 15 19. A liquid bleaching composition according to claim 1, wherein the organic substance comprises a pentadentate ligand.

20. A liquid bleaching composition according to claim 19, 20 wherein the pentadentate ligand is in the form of an iron complex.