Australian Patents Act 1990- Regulation 3.2A ORIGINAL COMPLETE SPECIFICATION STANDARD PATENT Invention Title "Ionic liquids comprising nitrogen containing cations" The following statement is a full description of this invention, including the best method of performing it known to me/us:- LIQUIDS This is a divisional of Australian patent application No. 2005232025, the entire contents of which are incorporated herein by reference. The present invention relates to ionic liquids and uses thereof. The invention also provides processes for the manufacture of ionic liquids. Ionic liquids are compounds which are composed of ions but which have a melting point below ambient temperature. They can be formed by a suitable combination of charge-delocalised, desymmetrised ions. The degree of order of the resulting salt can be reduced and the melting point lowered to a point where the resultant salt is liquid at ambient temperature. The delocalisation of the charge on the ion is also an important factor in determining the melting point of the resulting salt. Ionic liquids possess a number of remarkable properties, including negligible vapour pressure and high solvation capabilities, which have rendered them interesting alternatives to conventional solvents in a variety of applications. Ionic liquids may be made up of anions and cations or alternatively consist of zwitterions carrying both a positive and a negative charge on the same molecule. Most commonly the ionic liquid will comprise an anion and a cation. The prior art comprises liquids composed of a quaternary nitrogen- or phosphorus based cation, for example, based on a nucleus selected from quatemary ammonium cations, pyrrolidinium cations, imidazolium cations, triazolium cations, pyridinium cations, pyridazinium nations, pyrimidinium cations, pyrazinium cations and triazinium cations. These types of ionic liquids tend to be highly viscous, potentially hazardous and strongly absorb UV and visible light. Furthermore, the preparation of these ionic liquids involves a number of chemical and chromatographic steps that makes the process time consuming, expensive and inefficient. Anderson et al., J. Am. Chem. Soc. 124:14247-14254 (2002) discloses ionic liquids composed of a primary or tertiary ammonium based cation for use in certain chemical applications. 1 The inventors have provided further ionic liquids. According to the present invention there is provided an ionic liquid comprising an anion and a cation wherein the cation is a primary, secondary or tertiary- ammonium ion containing a charged nitrogen atom. As used herein a "primary ammonium ion" is an ammonium ion in which the nitrogen has 1 carbon atom attached to it. As used herein a "secondary ammonium ion" is an ammonium ion in which the nitrogen has 2 carbon atoms attached to it. As used herein a "tertiary ammonium ion" is an ammonium ion in which the nitrogen has 3 carbon atoms attached to it. According to a further aspect of the present invention there is provided an ionic liquid comprising an anion and a cation characterised in that the cation is a nitrogen containing cation of the formula (I) N'RRR'"I in which R is a hydrocarbyl group optionally substituted with by (-ne or more substituents selected from nitrogen-containing functional groups (including nitrile, nitro or amino or another basic nitrogen-containing functional group), thiel, alkythio, sulphonyl, thiocyanate, isothiocyanate, azido, hydrazino, halogen, alyl optionally interrupted by one or more ether or thioether linkages, alkoxy, alkenyl, hydroxy, carbonyl (including aldehyde or ketone), carboxyl, boronate, silyl and substituted amino (e.g. mono- or di-alkylamino or alkyamido); and R' and R", which may be the same or different, each represent H or R; 2 or any two or three of R, R' and R" may be joined together with the N to form a cyclic group. The term "ionic liquid" herein includes, but is not limited to, compounds consisting of ions and liquid at temperatures at which the compound is stable and the ionic liquids may have a melting point below 100*C, for example, below 25*C and optionally below 20 0 C. The boiling point of the ionic liquid may be at least 200*C. It may be above 500*C or even above 1000*C. The ionic liquids of the invention may consist entirely of ions, which. are liquid at the previously above defined temperatures in the dry state. Such itonic liquids will generally contain less than 1% water,.preferably less than 1000ppm water and more preferably still less than 1 00ppm water by mass. In a preferred aspect of the invention, ionic liquids are defined- as compounds consisting of a cation and an anion and having a water content of less than 100 parts per million. Preferably still, the ionic liquids have a melting point of 30*C or below, and a viscosity of less than 500 centipoise. For the purposes of this invention hydrocarbyl includes, but is not Limited to, alkyl, alkenyl, alkynyl, cyclohydrocarbyl, for example cycloalkyl, cycloalkemyl and moieties containing a combination thereof. As used herein "alkyl" relates to both straight chain and branched alkyl radicals, for example, of 1 to 12 carbon atoms, e.g. 1, 2, 3, 4, 5, 6, 7, 8 carbon atorns including but not limited to methyl, ethyl, n-propyl, isopropyl, n-butyl, sec-buty]l, isobutyl, tert butyl, n-pentyl, n-hexyl, n-heptyl, n-octyl. The term alkyl also encompasses cycloalkyl radicals including but not limited to cyclopropyl, cyclobutyl, cyclopentyl or cyclohexyl. 3 The alkyl group may be substituted with one or more halogen atoms. In one class of compounds the halogen is fluorine, in another it is chlorine, in a third it is a combination of fluorine and chlorine. "Alkoxy" relates to both straight chain and branched alkyl radicals, for example, of 1 to 12 carbon atoms, e.g. 1, 2, 3, 4, 5, 6, 7, 8 carbon atoms containing one or more oxygen atoms or hydroxyl. The term "alkenyl" means a straight or branched alkenyl radical of, for example, 2 to 12 carbon atoms, such as 2, 3, 4, 5 or 6 carbon atoms, and containing one or more carbon-carbon double bonds and includes but is not limited to ethylene, n-propyl-1 ene, n-propyl-2-ene, isopropylene etc. "Alkynyl" relates to a straight or branched alkynyl radical of, for example, 2 to 12 carbon atoms, such as 2, 3, 4, 5 or 6 carbon atoms, and containing one or more triple bonds. "Cyclohydrocarbyl" relates to a saturated, partly unsaturated or unsaturated 3 - 10, for example, 5, 6, 7, 8, 9 or 10, membered hydrocarbon ring, including cycloalkyl or aryl. "Aryl" means an aromatic, for example, 6 -10 membered hydrocarbon containing one, e.g. 6C-10C, ring which is optionally fused to one or more saturated or unsaturated rings, including phenyl or phenyl substituted by an alkyl or alkoxy group in which alkyl and alkoxy are as described herein. "Heteroaryl" means an aromatic, for example, 5-10 membered aromatic ring containing one or more heteroatoms selected from N, 0 or S, and containing one ring which is optionally fused to one or more saturated or unsaturated rings. 4 "Heterocyclyl" means, for example, a 3-10 membered ring system containing one qr more beteroatoms selected from N, 0 or S and includes heteroaryL The heterocyClyl system may contain one ring or may be fused to one or more saturated or unsaturated rings; the heterocyclyl may be fy saturated, partially satirated or unsaturated. "Cyclie group" means a ring or ring system, which may be unsaturated br partially unsaturated but is usually saturated, typically containing 5 to 13 ring-forming atoms, for example a 5-- or 6- membered ring. Examples include cyclohydrocarbyl or heterocyclyl. Examples of cyclohydrocarbyl or heterocyclyl groups include but are not limited to cyclohexyl, phenyl, acridine, benzimidazole, benzofuran, benzothiophefl4 benzoxazol, benzothiazole, carbazole, cinnoline, dioxin, dioxane, dioxolane, ditiane, ditiazine, ditiazole, dithiolane, thian, imidazole, imidazoline, imidazolidine, indole, indoline, indolizine, indazole, isoindole, isoqnioline, isooazole, isotbiazole, morpholiue, napthyxidine, oxazole. oxadiazole, oxathiazole, oxathiazoldine, oxazine, oxadiazine, phenazine, phenothiazine, phenoxane,a phthalazine, piperazine, piperidie, pteidiu, purine, putrescine, pyran, pyrazine, .pyrazole, pyrazoline, pyrazolidine, pyddazine, pyridine, .pyrhiidine, pyrolidine, pyrrole, pyrroliue, quinoline, quinoxabine, quinazoline, quinaolizine, tetrahydrofran, tetrazine, tetrazole, thiophene, thiadiazine, thiadiszole, tiatriazole, tbiazine, tlnazole, thiomorpholinmth ianaphthalene, thiopyran, triazine tiazole, tritiane, tropine. Halogen means F, 0, Br, or . 5 CWR~oin\llCCVdfu~dd@ t.DOC- I In another aspect of the invention there is provided the use, as a solvent, of an ionic liquid comprising an anion and a cation wherein the cation is a tertiary nitrogen-containing cation of the formula (1) N*HRR'R" (1) in which R is a hydrocarbyl group optionally interrupted by one or more ether or thioether linkages, and substituted with one or more substituents selected from nitrogen-containing functional groups; alkenyl, alkoxy, hydroxy; carbonyl and carboxyl groups; or from thiol, alkylthio, sulphonyl, thiocyanate, isothiocyanate, azido, hydrazino, halogen, boronate and silyl groups; and wherein R' and R", which may be the same or different, each represent a hydrocarbyl group optionally interrupted by one or more ether or thioether linkages, and optionally substituted with one or more substituents selected front: nitrogen-containing functional groups; alkyl, alkenyl, alkoxy, hydroxy; carbonyl and carboxyl groups; or from thiol, alkylthio, sulphonyl, thiocyanate, isothiocyanate, azido, hydrazino, halogen, boronate and silyl groups; or wherein any two or three of R, R' and R" may be joined together with the N to form a cyclic group. In one class of compounds R' and R" are 1L Compounds such as these having 1 R group and 3 hydrogens are referred to herein as primary ammonium ions. The invention covers compounds of formula (I) having 2 R groups and 2 hydrogens and which are referred to herein as secondary ammonium ions respectively. The 5A invention further covers compounds having 3 R groups and I hydrogen and which are referred to herein as tertiary ammonium ions. Included is a class of compounds in which R' and R" are different and have the same meaning as R. In a preferred aspect of the invention there is provided an ionic liquid consisting of an anion and a cation as defined in the first aspect of the invention. In a preferred aspect of the invention the cyclic group is a cyclohydrocarbyl or hetereocyclyl group, for example cyclohexylammonium. In one class of compounds there are excluded cations wherein any two or three of R, R', R" may be joined together with the N to form an aryl or heteroaryl group. Specifically excluded are pyridinium, pyrrolidinium and imidazolium cations. In one class of compounds where R is unsubstituted, there are excluded cations where R, R' and R" are the same and are ethyl or butyl. In one class of compounds wherein R, R' and/or R' is an unsubstituted hydrocarbyl group, the invention may include the following provisos: Where R is ethyl, the invention may include the proviso that R' and/or R" are not H. Where R' and R" are both CH 3 , the invention may include the proviso that R is not H. Where one or R' and R" is H and the other is CH 3 , the invention may include the proviso that R is not CH3. The invention may include the proviso that the ionic liquid is not any of the following: 6 Ethylammonium nitrate Tributylaninonium-acetate Tributylammoniuma-cyano-4-hydroxycinnamate Tributylamionium sinapate Dimethylanmonium pyridine-2-carboxylate Tributylammonium pyridine-2-carboxylate Tributylammonium 3-hydroxypyridine-2-carboxylate Triethylammonium pyridine-2-carboxylate In addition to demonstrating high solvation capability, the ionic liquids of the present invention have a low viscosity, are non-toxic and are colourless. These features make the ionic liquids of the present invention useful in a variety of applications. Preferably, R is substituted with a moiety selected from the group consisting of alkenyl, hydroxyl, amino, thio, carbonyl and carboxyl groups. More preferably, R is substituted with a hydroxyl or amino group. In one class of compounds, where R is substituted with a hydroxyl group, the invention may include the proviso that the ionic liquid is not dietbanolammonium chloride. If more than one substituent group (for example, selected from the group consisting of alkenyl, hydroxyl, amino, thiol, carbonyl and carboxyl groups) is present then more than one substituent group may be present on a single cation. In one class of compounds, R is a hydroxyalkyl group having 1, 2, 3, 4, 5 or 6 C atoms. The hydroxyalkyl group may have a hydroxyl moiety on its free, terminal carbon. R may be a polyol having 2 to 6 C atoms, for example, a di-alkanol, tri alkanol or tetra-alkanol group. 7 Preferably, the cation is an ethanolammonium. N-(alkoxyethyl)ammonium, N methylethanolarnmonium, NN-dimethylethanolammonium, diethanolammonium, N-alkyldiethanolammonium (e.g butyldiethanolammonium), NN di(alkoxyalkyl)ammonium (e.g di(methoxyethyl)ammonium) or triethanolammonium ion. More preferably the cation is a methylethanolammonium, N,N dimethylethanolammonium, N, N- di(methoxyethyl)ammonium) or butyldiethanolammonium ion. In another class of compounds, R is an aminoalkyl group having 2 to 8 C atoms, for example, 2, 3, 4, 5, 6, 7 or 8 C atoms. The aminoalkyl may be a di or tri-aminoalkyl group. In some compounds, R is putrescine, piperidine, or tropine. Preferred cations include an ethanolammonium, diethanolammonium, N butyldiethanolammonium, N-methylethanolammonium, di(methoxyethyl)aimmonium, NN-dimethylethanolarmonium, putrescinium, 1-(3 hydroxypropyl)putrescinium, or N-(3--hydroxypropyl)-N methylcyclohexylammonium ion. Preferably still, . cations include N butyldiethanolammonium, N-methylethanolammonium, I di(methoxyethyl)ammonium, NN-dimethylethanolammonium, putrescinium, 1-(3 hydroxypropyl)putrescinium, or N-(3-hydroxypropyl)-N methylcyclohexylammonium ion. Any cation included in the above list may be combined with any disclosed anion. The identity of the anions in the ionic liquids of the invention is not critical. The only theoretical constraint upon the choice of the anion is its ionic weight in order to keep the melting point of the ionic liquid below the desired temperature. 8 Preferably the anion is selected from halogenated inorganic anions, nitrates, sulphates, phosphates, carbonates, sulphonates and carboxylates. The sulphonates and carboxylates may be alkylsulphonates and alkylcarboxylates, in which the alkyl group is a moiety, for example having 1 to 20 C atoms, selected alkyl and alkyl substituted at any position with alkenyl, alkoxy, alkeneoxy, aryl, arylalkyl, aryloxy, amino, aminoalkyl, thio, thioalkyl, hydroxyl, hydroxyalkyl, carbonyl, oxoalkyl, carboxyl, carboxyalkyl or halide function, including all salts, ethers, esters, pentavalent nitrogen or phosphorus derivatives or stereoisomers thereof. For example, the anion may be selected from bis(trifluoromethylsulphonyl)imide, carbonate, hydrogen carbonate, sulphate, hydrogen sulphate, silicate, phosphate, hydrogen phosphate, dihydrogen phosphate, metaphosphate, methanesulphonate, trifluorornethanesulphonate, ethylenediaminetetraacetate, chloride, bromide, iodide, hexafluorophosphate, tetrafluoroborate, trifluoroacetate, pentafluoropropanoate, heptafluorobutanoate, oxalate, formate, acetate, propanoate, butanoate, pentanoate, hexanoate, heptanoate, octanoate, nonanoate, decanoate, benzoate, benezenedicarboxylate, benzenetricarboxylate, benzenetetracarboxylate, chlorobenzoate, fluorobenzoate, pentachlorobenzoate, pentafluorobenzoate salicylate, glycolate lactate, pantothenate, tartrate, hydrogen tartrate, mandelate, crotonate, malate, pyruvate, succinate, citrate, fannarate, phenylacetate. An especially preferred anion is an organic carboxylate. When the anion is required to include a labile proton then glycolate, tartrate and lactate anions are preferred. These contain both acid and hydroxyl functional groups. The ionic liquid according to the invention may contain cations which are all the same or which are different. In the same way, the ionic liquids may contain anions which are all the same or which are different. Thus the invention encompasses ionic liquids including a mixture of different cations and/or different anions. Ionic liquids of the invention may include any of the following: Ethanolammonium formate 9 Ethanolammonium acetate Ethanolammonium propanoate Ethanolammnonium propanedioate Ethanolammonium butanoate Ethanolammonium butenoate Ethanolammonium butanedioate Ethanolammonium pentanoate Ethanolarnmonium pentanedioate Ethanolammonium pentenoate Ethanolammonium hexanoate Ethanolammonium hexanedioate Ethanolammonium hexenoate Ethanolammonium heptanoate Ethanolanmonium heptanedioate Ethanolammonium heptenoate Ethanolanmonium octanoate Ethanolnmmonium octanedioate Ethanolanmmonium octenoate Ethanolarnmonium nonanoate Ethanolammonium nonanedioate Ethanolammonium nonenoate Etbanolammonium decanoate Ethanolammonium decanedioate Ethanolammonium decenoate Ethanolammonium undecanoate Ethanolammonium undecanedioate Ethanolammonium undecenoate Ethanolammonium dodecanoate Ethanolammonium dodecanedicarboxylate Ethanolammonium dodecenecarboxylate Ethanolamnonium cyclohexanecarboxylate 10 Ethanolammonium cyclohexenecarboxylate Ethanolammonium phenoxide Ethanolammonium benzoate Ethanolammonium benezenedicarboxylate Ethanolammonium benzenetricarboxylate Ethanolammonium benzenetetracarboxylate Ethanolammonium chlorobenzoate Ethanolammonium fluorobenzoate Ethanolammonium pentachlorobenzoate Ethanolammonium pentafluorobenzoate Ethanolammionium salicylate Ethanolammonium glycolate Ethanolammonium lactate Ethanolammonium pantothenate Ethanolammonium tartrate Ethanolammonium hydrogen tartrate Ethanolammonium mandelate Ethanolammonium crotonate Ethanolammonimin malate Ethanolammonium pyruvate Ethanolammonium succinate -- Ethanolammonium citrate Ethanolammonium fumarate Ethanolammonium phenylacetate Ethanolammonium oxalate Ethanolammonium bis(trifluoromethylsulphonyl)imide Ethanolammonium carbonate Ethanolammonium hydrogen carbonate Ethanolammonium sulphate Ethanolammonium hydrogen sulphate Ethanolammonium phosphate 11 Ethanolammonium hydrogen phosphate Ethanolammonium dihydrogen phosphate Ethanolammnonium methanesulfonate Ethanolamonanium trifluoromethanesulphonate Ethanolammonium ethylenediaminetetraacetate Ethanolammonium hexafluorophosphate Ethanolammonium tetrafluoroborate Ethanolammonium trifluoroacetate Ethanolammonium pentafluoropropanoate Ethanolammonium heptafluorobutanoate Ethanolammonium phosphoenolpyruvate Ethanolammonium nicotinamide adenine dinucleotide phosphate Ethanolammonium adenosinephosphate Ethanolammonium adenosine diphosphate Ethanolammonium adenosine triphosphate Ethanolammonium oxyniacate Ethanolammonium nitrate Ethanolammonium nitrite Diethanolammonium bromide Diethanolammonium iodide Diethanolammonium formate Diethanolammonium acetate Diethanolammonium propanoate Diethanolammonium propanedioate Diethanolammonium butanoate Diethanolammonium butenoate Diethanolammonium butanedioate Diethanolammonium pentanoate Diethanolammonium pentanedioate Diethanolammonium pentenoate Diethanolammonium hexanoate 12 Diethanolammoniuma hexanaedioate Diethanolaniinonium hexenoate Diethanolammonium heptanoate Diethanolammoniuma heptanedioate Diethanolaminonium hepteno ate Diethanolammonium octanoate Diethanolaminonium octanedloate Dietlaanolammonium octenoate Diethanolamnaonium nonanoate Diethanolammonium nonanedioate Diethanolammonium nonenoate Diethanolammonium decanoate Diethanolammonium decanedloate Diethanolammonium decenoate Diethanolammonium undecanoate Diethanolammonium iindecanedioate Diethanolammonium undecenoate Diethanolaminonium dodecanoate Diethanolammonium dodecanedicarboxylate Diethanolammoniumir dodecenecarboxylaie Dietbanolammonium cyclohexanecarboxylate Diethanolammonium cyclohexenecarboxylate Diethanolammonium phenoxide Diethanolamnaoniuma benzoate Diethanolammoniuma benezenedicarboxylate Diethanolammoniuin benzenetricarboxylate Diethanolammnonium benzenetetracarboxylate Diethanolamnaoniuna cblorobenzoate Diethanolammaoniun fluorobenzoate Diethanolammoniuni pentacblorobenzoate Diethanolaminonium pentafluorobenzoate 13 Diethanolammonium salicylate Diethanolammonium glycolate Diethanolammonium lactate Diethanolammonium pantothenate Diethanolammonium tartrate Diethanolammonium hydrogen tartrate Diethanolammonium mandelate Diethanolammonium crotonate Diethanolammonium malate Diethanolammonium pyruvate Diethanolanmonium succinate Diethanolammonium citrate Diethanolammonium fumarate Diethanolammonium phenylacetate Diethanolammonium oxalate Diethanolammonium bis(trifluoromethylsulphonyl)imide Diethanolammonium carbonate Diethanolammonium hydrogen carbonate Diethanolammonium phosphate. Diethanolammonium hydrogen phosphate Diethanolammonium dihydrogen phosphate Diethanolammonium methanesulphonate Diethanolammonium trifluoromethanesulphonate Diethanolammoniuna ethylenediaminetetraacetate Diethanolammonium hexafluorophosphate Diethanolammonium tetrafluoroborate Diethanolammonium trifluoroacetate Diethanolammonium pentafluoropropanoate Diethanolammonium heptafluorobutanoate Diethanolammonium phosphoenolpyruvate Diethanolammonium nicotinamide adenine dinucleotide phosphate 14 Diethanolammonium adenosinephosphate Diethanolammoni-um adenosine diphosphate Diethanolammonium adenosine triphosphate Diethanolammonium oxyniacate Diethanolammonium nitrate Diethanolammonium nitrite N-Butyldiethanolammonium chloride N-Butyldiethanola-monium bromide N-Butyldiethanolammonium iodide N-Butyldiethanolaxmmonium formate N-Butyldiethanolamnmonium acetate N-Butyldiethanolamnmonium propanoate N-Butyldiethanolaimmonium propanedioate N-Butyldiethanolammonium butanoate N-Butyldiethanolammonium butenoate N-Butyldiethanolamnmonium butanedioate N-Butyldiethanolammaonium pentanoate N-Butyldiethanolamnmonium pentanedioate N-Butyldiethanolammonium pentenoate N-Butyidiethanolammonium hexanoate N-Butyldiethanolammonium hexenoate N-Butyldiethanolammonium heptanoate N-Butldiethanola~mnonium heptanedioate N-Butyldiethanolammonium heptenoate N-Butyldiethanolammonium octanoate N-Butyldiethanolammonium octanedloate N-Butyldiethanolammonium octenoate N-Butyldiethanolammonium nonanoate N-Butyldiethanolanmonium nonanedioate N-Butyldiethanolammonium nonenoate N-Butyldiethanolammonium decanoate 15 N-Butyldiethanolammonium decanedioate N-Butyldiethanolanimonium decenoate N-Butyldiethanolammonium undecanoate N-Butyldiethanolammonium undecanedioate N-Butyldiethanolammonium undecenoate N-Butyldiethanolammonium dodecanoate N-Butyldiethanolammoniium dodecanedicarboxylate N-Butyldiethanolammonium dodecenecarboxylate N-Butyldiethanolammonium cyclohexanecarboxylate N-Butyldiethanolammonium cyclohexenecarboxylate N-Butyldiethanolammoniurm phenoxide N-Butyldiethanolammonium benzoate N-Butyldiethanolammonium benezenedicarboxylate N-Butyldiethanolammonium benzenetricarboxylate N-Butyldiethanolammonium benzenetetracarboxylate N-Butyldiethanolammonium chlorobenzoate N-Butyldiethanolammonium fluorobenzoate N-Butyldiethanolammonium pentachlorobenzoate N-Butyldiethanolammonium pentafluorobenzoate N-Butyldiethanolammonium salicylate N-Butyldiethanolammonium glycolate N-Butyldiethanolammonium lactate N-Butyldiethanolammonium pantothenate N-Butyldiethanolammonium tartrate N-Butyldiethanolammonium hydrogen tartrate N-Butyldiethanolammonium inandelate N-Butyldiethanolammonium crotonate N-Butyldiethanolammonium malate N-Butyldiethanolammonium pyruvate N-Butyldiethanolammonium succinate N-Butyldiethanolammonium citrate 16 N-Butyldiethanolammonium fumarate N-Butyldiethanolammonium phenylacetate N-Butyldiethanolaimmonium oxalate N-Butydiethanolammonium bis(trifluoromethylsulphonyl)imide N-Butyldiethanolanunonium carbonate N-Butyldiethanolammonium hydrogen carbonate N-Butyldiethanolammonium sulphate N-Butyldiethanolanmonium hydrogen sulphate N-Butyldiethanolammonium phosphate N-Butyldiethanolammonium hydrogen phosphate N-Butyldiethanolammonium dibydrogen phosphate N-Butyldiethanolammonium methanesulphonate N-Butyldiethanolammonium trifluoromethanesulphonate N-Butyldiethanolammonium ethylenediaminetetraacetate N-Butyldiethanolammonium hexafluorophosphate N-Butyldiethanolammonium tetrafluoroborate N-Butyldiethanolammonium trifluoroacetate N-Butyldiethanolammonium pentafluoropropanoate N-Butyldiethanolammonium heptafluorobutanoate N-Butyldiethanolammonium phosphoenolpyruvate N-Butyldiethanolammonium nicotinamide adenine dinucleotide phosphate N-Butyldiethanolammonium adenosinephosphate N-Butyldiethanolammonium adenosine diphosphate N-Butyldiethanolammonium adenosine triphosphate N-Butyldiethanolammonium oxyniacate N-Butyldiethanolammonium nitrate N-Butyldiethanolammonium nitrite N,N-Dimethylethanolammonium bromide N,N-Dimethylethanolammonium iodide N,N-Dimethylethanolammonium formate N,N-Dimethylethanolammonium acetate 17 N,N-Dimethylethanolainmoniuma propanoate N,N-Dimethylethanolammonium propanedioate N,N-Dimethylethanolarnonium butanoate N,N-Dirnethylethanolanimonium butenoate N,N-Dimethylethanolammonium butanedloate N,N-Diinethylethanolammoniuni penatano ate N,N-Dimethylethanolaininoniuin pentanedioate N,N-Dimethylethanolaqmmonium pentenoate N,N-Dinaethylethaaolanmmonium hexanoate N,N-Dinlethylethanolaqnmonium hexenoate N,N-Dimethylethanolannnonium heptanoate N,N-Dimethylethanolammoniui heptanedioata N,N-Dimethylethanolammonium heptenoate N,N-Dimethylethanolanunonium octanoate N,N-Dimethylethanolammonium octanedioate N,N-Dhnethylethanolammonium octenoate N,N-Dinaethyledbaolammonium nonanoate N,N-Diimethylethanolammonium nonanedloate N,N-Dimethylethanolammonium nonenoate N,N-Dimethylethanolammonium decanoate N,N-Diinethyletbanolammonium decanedloate N,N-Dimnethylethanolammonium decenoate N,N-Dimethylethanolammonium undecanoate NN-Dimethylethanolammoniuma undecanedioate N,N-Dimethylethanolaimonium undecenoate N,N-Dinaethylethanolammonium dodecanoate N,N-Dinaethylethanolammonium dodecanedicarboxylate N,N-Dimethylethanolammonium dodecenecarboxylate N,N-Dinaethylethanolammoniuma cyclohexanecarboxylate N,N-Dinaethylethanolagmmonium cyclohexenecarboxylate N,N-Dimethylethanolammoniumn phenoxide 18 N,N-Dimethylethanolammonium benzoate N,N-Dimethylethanolammonium benezenedicarboxylate N,N-Dimethylethanolammonium benzenetricarboxylate N,N-Dimethylethanolarmnonium benzenetetracarboxylate N,N-Dimethylethanolammonium chlorobenzoate N,N-Dimethylethanolammoniun fluorobenzoate N,N-Dimethylethanolanmmonium pentachlorobenzoate N,N-Dimethylethanolammonium pentafluorobenzoate N,N-Dimethylethanolammonium salicylate N,N-Dimethylethanolammonium glycolate N,N-Dimethylethanolammonium lactate N,N-Dimethylethanolammonium pantothenate N,N-Dimethylethanolammonium tartrate N,N-Dimethylethanolammonium hydrogen tartrate N,N-Dimethylethanolammonium mandelate N,N-Dimethylethanolammonium crotonate N,N-Dimethylethanolammonium malate N,N-Dimethylethanolammonium pyruvate N,N-Dimethylethanolammonium succinate N,N-Dimethylethanolammonium citrate N,N-Dimethylethanolammonium fumarate N,N-Dimethylethanolammonium phenylacetate N,N-Dimethylethanolammonium oxalate N,N-Dimethylethanolammonium bis(trifluoromethylsulphonyl)imide N,N-Dimethylethanolammonium carbonate N,N-Dimethylethanolammonium hydrogen carbonate N,N-Dimethylethanolammonium sulphate N,N-Dimethylethanolammonium hydrogen sulphate N,N-Dimethylethanolammonium phosphate N,N-Dimethylethanolammonium hydrogen phosphate N,N-Dimethylethanolammonium dihydrogen phosphate 19 N,N-Dimethylethanolammonium methanesulphonate N,N-Dimethylethanolammonium trifluoromethanesulphonate -NN-Diiiefy-leisiiolan'm-iidinn etylEnedianim tt estate N,N-Dinaethylethanolammonium hexafluorophosphate N,N-Dinaethylethanolammonium tetrafluoroborate N,N-Dinmethylethanolammonium trifluoroacetate N,N-Dinaethylethanolammonium pentafluoropropanoate N,N-Dinaethylethanolammonium heptafluorobutanoate N,N-Diiaethylethanolammonium phosphoenolpyruvate N,N-Dinaethylethanolammonium nicotinamide adenine dinucleoticle phosphate N,N-Diniethylethanolammonium adenosinephosphate N;N-Dinaethylethanolammonium adenosine diphosphate N,N-Diniethylethanolammonium adenosine triphosphate N,N-Diniethylethanolammonium oxyniacate N,N-Dinethylethanolammonium nitrate N,N-Dinethylethanolammonium nitrite N-Methylethanolammonium bromide N-Methylethanolammonium iodide N-Methylethanolammonium formate N-Methylethanolammonium acetate N-Methylethanolammonium propanoate N-Methylethanolammonium propanedioate N-Methylethanolammonium butanoate N-Methylethanolamonium butenoate N-Methylethanolammonium butanedioate N-Methylethanolammonium pentanoate N-Methylethanolammonium pentanedioate N-Methylethanolammonium pentenoate N-Methylethanolammonium hexanoate N-Methylethanolammonium hexenoate N-Methylethanolammonium heptanoate 20 N-Methylethanolammionium heptanedio ate N-Methylethanolammonium heptenioate N-Methylethanolammonium octanoate N-Methylethanolammonium octanedioate N-Methylethanolammonium octenoate N-Methylethanolammonium nona noate *N-Metliylethanolaqmmonium nonanedloate N-Methylethanolanimonium nonenoate N-Methylethanolaxnnaonium decanoate N-Methylethanolaminonium decanedioate N-Methylethanolammonium decenoate N-Methylethanolamnmonium undecanoate N-Methylethanolammonium undecanedioate N-Methylethanolammionium undecenoate N-Methylethanolammonium dodecanoate N-Methylethanolammonium dodecanedicarboxylate N-Methylefbanolammonium dodecenecarboxylate N-Methylethiaiolammoniumr cyclohexanecarboxylate N-Metbylethai-qolarmonium cyclohexenecarboxylate N-Methylethacnolananium phenoxide N-Metliylethamnolammonium benzoate N-Methylethanolammonium benezenedicarboxylate N-Methylethaiaolammonium benzenetricarboxylate N-Methyletbaaolammonium beazenetefracarboxylate N-Methylethamnolammoniuni chlorobenzoate N-Methylethaiiolamnaonium fluorobeazoate N-Methylethamolammonium pentacblorobenzoate N-Methylethamolammonium pentafluorobeuzoate N-Methylethmuolammonium salicylate N-Methylethanolammonium glycolate N-Methylethmiolammoniuna lactate 21 N-Methylethanolammonium pantothenate N-Methylethanolammonium tartrate N-Methylethanolammonium hydrogen tartrate N-Methylethanolammonium mandelate N-Methylethanolammonium crotonate N-Methylethanolammonium malate N-Methylethanolammonium pyruvate N-Methylethanolammonium succinate N-Methylethanolammonium citrate N-Methylethanolammonium fumarate N-Methylethanolammonium phenylacetate N-Methylethanolaimonium oxalate N-Methylethanolammonium bis(trifluoromethylsulphonyl)imide N-Methylethanolammonium carbonate N-Methylethanolammonium hydrogen carbonate N-Methylethanolammonium sulphate N-Methylethanolammonium hydrogen sulphate N-Methylethanolammonium phosphate N-Methylethanolammonium hydrogen phosphate N-Methylethanoiammonium dihydrogen _phosphate N-Methylethanolammonium methanesulphonate N-Methylethanolammonium trifluoromethanesulphonate N-Methylethanolammonium ethylenediarninetetraacetate N-Methylethanolammonium hexafluoroplosphate N-Methylethanolammonium tetrafluoroborate N-Methylethanolammonium trifluoroacetate N-Methylethanolannmonium pentafluoropropanoate N-Methylethanolammonium heptafluorobutanoate N-Methylethanolammonium phosphoenolpyruvate N-Methylethanolammonium nicotinamide adenine dinucleotide phosphate N-Methylethanolammonium adenosineph.osphate 22 N-Methylethanolammonium adenosine diphosphate N-Methylethanolammonium adenosine triphosphate N-Methylethanolammonium oxyniacate N-Methylethanolammonium nitrate N-Methylethanolammonium nitrite N,N-Di(methoxyethyl)ammonium chloride N,N-Di(methoxyethy)ammonium bromide N,N-Di(methoxyethyl)ammonium iodide N,N-Di(methoxyethyl)ammonium formate N,N-Di(methoxyethyI)ammonium acetate N,N-Di(methoxyethyl)ammonium propanoate N,N-Di(methoxyethyl)ammonium propanedioate N,N-Di(methoxyethyl)ammonium butanoate N,N-Di(methoxyethyl)ammonium butenoate N,N-Di(methoxyethyl)ammonium butanedioate N,N-Di(methoxyethyl)ammonium pentanoate N,N-Di(methoxyethy)ammonium pentanedioate N,N-Di(methoxyethyl)ammonium pentenoate N,N-Di(methoxyethyl)ammonium hexanoate N,N-Di(methoxyethyi)ammonium hexenoate N,N-Di(methoxyethyl)ammonium heptanoate N,N-Di(methoxyethyl)ammonium heptanedioate N,N-Di(methoxyethyl)ammonium heptenoate N,N-Di(methoxyethyl)ammonium octanoate N,N-Di(methoxyethyl)ammonium octanedioate N,N-Di(methoxyethyl)ammonium octenoate NN-Di(methoxyethyl)ammonium nonanoate NN-Di(methoxyethyl)ammonium nonanedioate N,N-Di(methoxyethyl)ammonium nonenoate N,N-Di(methoxyethyl)ammonium decanoate N,N-Di(methoxyethyl)ammonium decanedioate 23 N,N-Di(methoxyethyl)ammonium decenoate N,N-Di(methoxyethyl)ammonium undecanoate N,N-Di(methoxyethyl)ammonium undecanedioate N,N-Di(methoxyethyl)ammonium undecenoate N,N-Di(methox-yethyl)ammonium dodecanoate N,N-Di(methoxyethyl)ammonium dodecanedicarboxylate N,N-Di(methoxyethyl)ammonium dodecenecarbox-ylate N,N-Di(methoxyethyl)ammonium cyclohexanecarboxylate N,N-Di(methoxyethyl)ammonium cyclohexenecarboxylate N,N-Di(methoxyethyl)ammonium phenoxide N,N-Di(methoxyethyl)ammonium benzoate N,N-Di(methoxyethyl)ammonium benezenedicarboxylate N,N-Di(methoxyethyl)ammonium benzenetricarboxylate N,N-Di(methoxyethyl)ammonium benzenetetracarboxylate N,N-Di(methoxyethyl)ammonium chlorobenzoate N,N-Di(methoxyethyl)ammonium fluorobentoate N,N-Di(methoxyethyl)ammonium pentachlorobenzo>ate N,N-Di(methoxyethyl)ammonium pentafluorobenzoate N,N-Di(methoxyethyl)atnmonium salicylate N,N-Di(methoxyethyl)ammonium glycolate N,N-Di(methoxyethyl)ammonium lactate N,N-Di(methoxyethyl)ammonium pantothenate N,N-Di(methoxyethyl)ammonium tartrate N,N-Di(methoxyethyl)amnonium hydrogen tartrate N,N-Di(methoxyethyl)ammonium mandelate N,N-Di(methoxyethyl)ammonium crotonate N,N-Di(methoxyethyl)ammonium malate N,N-Di(methoxyethyl)ammonium pyruvate N,N-Di(methoxyethyl)ammonium succinate N,N-Di(methoxyethyl)ammonium citrate N,N-Di(methoxyethyl)ammonium fumarate 24 N,N-Di(methoxyethyl)ammonium phenylacetate N,N-Di(methoxyethyl)ammonium oxalate N,N-Di(methoxyethyl)ammonium bis(trifluoromethylsulphonyl)imice N,N-Di(methoxyethyl)ammonium carbonate N,N-Di(methoxyethyl)ammonium hydrogen carbonate N,N-Di(methoxyethyl)ammonium sulphate N,N-Di(methoxyethyl)ammonium hydrogen sulphate N,N-Di(methoxyethyl)ammonium phosphate N,N-Di(methoxyethyl)ammonium hydrogen phosphate N,N-Di(methoxyethyl)amrnonium dihydrogen phosphate N,N-Di(methoxyethyl)ammonium methanesulphonate N,N-Di(methoxyethyl)ammonium trifluoromethanesulphonate N,N-Di(methoxyethyl)ammonium ethylenediaminetetraacetate N,N-Di(methoxyethyl)ammonium hexafluorophosphate N,N-Di(methoxyethyl)ammonium tetrafluoroborate N,N-Di(methoxyethyl)ammonium trifluoroacetate N,N-Di(methoxyethyl)ammonium pentafluoropropanoate N,N-Di(methoxyethyl)ammonium heptafluorobutanoate N,N-Di(methoxyethyl)ammonium phosphoenolpyruvate N,N-Di(methoxyethyl)ammouium niicotinamide adenine dinucleotide phosphate N,N-Di(methoxyethyl)ammonium adenosinephosphate N,N-Di(methoxyethyl)ammonium adenosine diphosphate N,N-Di(methoxyethyl)ammonium adenosine triphosphate N,N-Di(methoxyethyl)ammonium oxyniacate N,N-Di(methoxyethyl)ammonium nitrate N,N-Di(methoxyethyl)ammonium nitrite 1-(3-Hydroxypropyl)putrescinium chloride 1-(3-Hydroxypropyl)putrescinium bromide 1-(3-Hydroxypropyl)putrescinium iodide 1-(3-Hydroxypropyl)putrescinium fonnate 1-(3-Hydroxypropyl)putrescinium acetate 25 1 -(3-Hyd-roxypropyl)putescinium propanoate 1 -(3 -Hydrox-ypropyl)puttescinium propanedioate 1 -(3-Hydrox-ypropy)putrescinium butanoate 1 -(3-1{ydroxypropyl)putrescinium butenoate 1 -(3 -Hydroxypropyl)putrescinium butanedioate 1 -(3 -Hydroxypropyl)putrescinium pentanoate 1 -(3 -Hydroxypropyl)putrescinium pentanedioate 1 -(3 -Hydroxypropyl)putrescinium pentenoate 1-(3-Hydroxypropyl)putrescinium hexanoate I -(3 -Hydroxypropyl)putresciniumm hexenoate 1-(3-Hydroxypropyl)putresciniuin heptanoate 1-(3-Hydrox3propyl)putrescinium heptanedioate 1 -(3 -Hydroxypropyl)putrescinium heptenoate 1-(3-Hydroxypropyl)putrescinium octanoate 1-(3-Hydroxypropyl)pulresciniuim octanedloate 1-(3-Hydroxypropyl)putresciniuim octenoate 1-(3-Hydroxypropyl)putrescinium nonanoate 1-(3-Hydroxypropyl)putrescinium nonanedioate 1.(3-Hydroxyopyl)putrescinium nonenoate 1-(3-Hydroxypropyl)putrescinium decanoate 1-(3-Hydroxypropyl)putrescinium decanedioate . 1-(3-Hydroxypropyl)putrescinium decenoate 1-(3-Hydroxypropyl)putrescinium undecanoate 1 -(3-Hydroxypropyl)putrescinium undecanedioate 1 -{3-Hydroxypropyl)putrescinium 'tmdecenoate 1-(3-Hydroxypropyl)putresciniuim dodecanoate 1 -(3 -Hydroxypropyl)putrescinium dodecanedicarboxylate 1-(3-Hydroxypropyl)putresciuium dodecenecarboxylate 1 -(3-Hydroxypropyl)putresciniuim cyclohexanecarboxylate 1 -(3 -Hydroxypropyl)putrescinium cyclohexenecarboxylate 1-(3-Hydroxypropyl)putrescinium phenoxide 26 1-(3-Hydroxypropyl)putrescinium benzoate 1-(3-Hydroxypropyl)putrescinium benezenedicarboxylate 1-(3-Hydroxypropyl)putrescinium benzenetricarboxylate 1-(3-Hydroxypropyl)putrescinium benzenetetracarboxylate 1-(3-Hydroxypropyl)putrescinium chlorobenzoate 1-(3-Hydroxypropyl)putrescinium fluorobenzoate 1-(3-Hydroxypropyl)putrescinium pentachlorobenzoate 1-(3-Hydroxypropyl)putrescinium pentafluorobenzoate 1-(3-Hydroxypropyl)putrescinium salicylate 1-(3-Hydroxypropyl)putrescinium glycolate 1-(3-Hydroxypropyl)putrescinium lactate 1-(3-Hydroxypropyl)putrescinium pantothenate 1-(3-Hydroxypropyl)putrescinium tartrate 1-(3-Hydroxypropyl)putrescinium hydrogen tartrate 1-(3-Hydroxypropyl)putrescinium inmandelate 1-(3-Hydroxypropyl)putrescinium crotonate 1-(3-Hydroxypropyl)putrescinium malate 1-(3-Hydroxypropyl)putrescinium pyruvate 1-(3-Hydroxypropyl)putrescinium succinate 1-(3-Hydroxypropyl)putrescinium citrate 1-(3-Hydroxypropyl)putrescinium fumarate 1-(3-Hydroxypropyl)putrescinium phenylacetate 1-(3-Hydroxypropyl)putrescinium oxalate 1-(3-Hydroxypropyl)putrescinium bis(trifluoromethylsulphonyl)imide 1-(3-Hydroxypropyl)putrescinium methanesulphonate 1-(3-Hydroxypropyl)putrescinium trifluoromethanesulphonate 1-(3-Hydroxypropyl)putrescinium hexafluorophosphate 1-(3-Hydroxypropyl)putrescinium tetrafluoroborate 1-(3-Hydroxypropyl)putrescinium trifluoroacetate 1-(3-Hydroxypropyl)putrescinium pentafluoropropanoate 1-(3-Hydroxypropyl)putrescinium heptafluorobutanoate 27 1-(3-Hydroxypropyl)putresciniun phosphoenolpyruvate 1-(3-Hydroxypropyl)putrescinium nicotinamide adenine dinucleotide phosphate 1-(3-Hydroxypropyl)putrescinium adenosinephosphate 1-(3-Hydroxypropyl)putrescinium adenosine diphosphate 1-(3-Hydroxypropyl)putrescinium adenosine triphosphate 1-(3-Hydroxypropyl)putrescinium carbonate 1-(3-Hydroxypropyl)putrescinium hydrogen carbonate 1-(3-Hydroxypropyl)putrescinium sulphate 1-(3-Hydroxypropyl)putrescinium hydrogen sulphate 1-(3-Hydroxypropyl)putrescinium phosphate 1-(3-Hydroxypropyl)putrescinium hydrogen phosphate 1-(3-Hydroxypropyl)putrescinium dihydrogen phosphate 1-(3-Hydroxypropyl)putrescinium nitrate 1-(3-Hydroxypropyl)putrescinium nitrite In one class of compounds, the invention includes the proviso that the ionic liquid is not ethylammonium nitrate or diethanolammonium chloride. In a further class of compounds, the invention includes the proviso that the ionic liquid is not a N protonated pyridimium or pyrrolidinium salt. According to a further aspect, the present invention provides a process for the preparation of an ionic liquid according to the invention, the process comprising the steps of: i.) providing an organic primary, secondary or tertiary amine; and ii.) neutralising the compound in (i) with an acid. The process according to the invention may comprise the steps of: i.) providing a nitrogen-containing compound of the formula (II) NRR'R" (11) in which R, R' and R" have the meaning defined herein; and ii.) neutralising the compound in (i) with an acid. 28 The process of the present invention provides an economical route to the manufacture of ionic liquids since the process involves only a single step and uses starting materials that are generally readily available. During the process of the invention, the nitrogen atom of the primary, secondary or tertiary amine is protonated to provide a protonated ammonium ion. Preferably, the acid includes an anion as defied herein. Preferably the acid anion- comprises a halogenated inorganic anion, nitrate, sulphate, carbonate, sulphonate or carboxylate. The invention also encompasses compounds of formula (II) and their use in the preparation of one or more ionic liquids. The invention further provides the use of a cation as defined in the ionic liquids of the present invention in a solvent for enzyme-catalysed reactions. Further provided is the use of an ionic liquid according to tihe present invention as a solvent for enzyme catalysed reactions. The use of ionic liquids in certain biological and/or chemical reactions has several advantages over traditional aqueous solutions. Ionic liquids have an ability to dissolve a wide range of inorganic, organic, polymeric and biological materials, often to a very high concentration. They have a wide liquid range, allowing both high and low temperature processes to be carried out in the same solvent. They do not elicit solvolysis phenomena and most stabilise short-lived reactive intermediates. There are no pH effects in the solvents and there is practically zero vap-our pressure over much of the liquid range. Ionic liquids also exhibit excellent electrical and thermal conductivity whilst being non-flammable, recyclable and generally of low toxicity. 29 The invention further provides the use of an ionic liquid, or of a cation as defied in an ionic liquid, according to the present invention in a solvent for organic synthesis, matrixes in matrix-assisted laser desorption/ionisation (MALDI) mass spectrometry, solvent extraction (e.g to remove desired components from an immiscible liquid or solid) or gas chromatography, catalysis, liquefaction, nuclear fuel reprocessing, fuel cells, electrochemical applications, pervaporation, drug delivery, lubrication, hydraulic fluids, adhesives, sensors, biocides and chromatographic media. Further provided is a method for carrying out an enzyme-catalysed reaction comprising i.) providing a liquid reaction medium which comprises an ionic liquid according to the present invention; ii.) providing in the liquid reaction medium an enzyme and a substrate for the enzyme; and iii.) allowing reaction of the substrate to occur. Further provided is a method for the synthesis of one or more organic compounds, the method comprising carrying out an organic synthesis reaction in an ionic liquid according to.the present invention. Throughout the description and claims of this specification, the words "comprise" and "contain" and variations of the words, for example "comprising" and "comprises", means "including but not limited to", and is not intended to (and does not) exclude other moieties, additives, components, integers or steps. Throughout the description and claims of this specification, the singular encompasses the plural unless the context otherwise requires. In particular, where the indefinite article is used, the specification is to be understood as contemplating plurality as well as singularity, unless the context requires otherwise. Features, integers, characteristics, compounds, chemical moieties or groups described in conjunction with a particular aspect, embodiment or example of the invention are 30 to be understood to be applicable to any other aspect, embodiment or example described herein unless incompatible therewith. The invention will now be described by way of the following, non-limiting examples: MATERIALS AND METHODS Preparation of ammonium-based ionic liquids bearing one or more ammoniacal protons The requisite stoichiometric equivalents of the parent amine and complementary acid were dissolved independently in water, methanol or ethanol to give solutions of equal concentrations. Equal volumes of these two solutions were mixed together in a flask, with stirring and cooling, at a rate sufficiently slow as to prevent the temperature of the reaction from exceeding 60*C. When neutralization was complete, the excess solvent was removed in vacuo, at temperatures not exceeding 60*C. The product was then freeze-dried, analysed and stored in a desiccated condition. Preparation ofNN-dinethylethanolamznzoniumi glycolate Alcoholic solutions of NN-dimethylethanolamine (100.OOmL, 2.OOOM concentration) and glycolic acid (100.OOmL, Z.OOOM concentration) were gradually mixed together in a 500mL round-bottomed flask, with external cooling and stirring. Afler. completion of the neutralisation reaction, the cold alcoholic solution. was filtered, transferred to a clean flask and the solvent was removed on a rotary evaporator. The reaction product was frozen in liquid nitrogen and lyophilised in vacuo, being gradually permitted to rise to room temperature, to yield 32.85g (99%) of a pale yellow liquid, water content <100ppm by Karl Fischer titration, purity > 99.9% by ion chromatography. The product was analysed by elemental analysis and by infra-red, ultra-violet/visible and nuclear magnetic resonance spectroscopy and was stored over anhydrous calcium chloride in a vacuum desiccator. 31 FT-IR (cm-'): 1591, 1076, 1358, 687, 993, 1468, 909,1255, 881, 1154,1171, 3240, 2870, 2484, 1745 UVIvis X.,_, (nm): 234 ENT (Reichardt): 0.912 Density (g cn-3): 1.146 Preparation ofN-buildiethanolannonium bis(trifluoronethylsulphonyl)imide To an alcoholic solution of N-butyldiethanolamine (100.OOmL, 2.000M concentration) in a 500mL round-bottomed flask was gradually added 56.232g bis(trifluoromethylsulphonyl)imide, with vigorous stirring and extemal cooling, over a period of 30 minutes. After completion of the reaction, the solution was filtered and the solvent was removed in vacuo. The product was dried as above to yield 87.2g (98%) of a pale yellow liquid, water content <100ppm by Karl Fischer titration, purity >98% by ion chromatography . The product was analysed and stored as previously described. FT-IR (cm-l):1051, 1132, 1181, 1347, 741, 791, 764, 880,960, 1461, 2967, 3523, 2941, 2880, 3138, 1632 UV/vis X. (nm): 304 ENT (Reichardt): 0.994 Density (g cm.
3 ): 1.343 APPLICATIONS Enzyme-catalysed reaction in NN-dinethylethanolanmoniun glycolate Alcohol dehydrogenase: Methanol (50pL) was dissolved in the ionic liquid (6mL) with a net water content of <1 00ppm by Karl Fischer titration. Nicotinamide adenine dinucleotide (100mg) was added along with lyophilised Saccharoiyces cerevisiae alcohol dehydrogenase (1mg). The reaction vessel was sealed and incubated at 30*C 32 for 24 hours, with vigorous shaking being maintained throughout. Samples (lmL) were extracted at time points of 0, 2, 4, 8, 12 and 24 houts and were analysed by means of the chromotropic acid assay. The absorbance of the analyte samples at 560nm was measured against enzyme-free standards and correlated with the concentration of formaldehyde by comparison with a standard curve. The accumulation of formaldehyde was observed up to an equilibrium concentration of 20+/-2mM. Biodegradation ofN,N-dimethylethanolammonium glycolate N,N-Dimethylethanolammonium glycolate (5mM) was used as sole nitrogen and carbon source for the selective enrichment of a mixed community of soil..micro organism collected from waste ground. Individual organims were isolated from the mixed culture and were screened for their capability to metabolise the ionic liquid at varying concentrations in aqueous phosphate buffer. Experiments were performed in Erlenmeyer flasks at 30 0 C, with shaking at llOrpm. Degradation was monitored using ion chromatography. 5mM Ionic liquid was readily degraded (>98% removal) within 48 hours, the final nitrogenous metabolite being ammonia. The reference in this specification to any prior publication (or information derived from it), or to any matter which is known, is not, and should not be taken as an acknowledgment or admission or any form of suggestion that that prior publication (or information derived from it) or known matter forms part of the common general knowledge in the field of endeavour to which this specification relates. 33