Patent Application
20240317690
The technical field generally relates to salts for use in electrolyte compositions or as additive in electrode material, and to methods for the preparation. The technical field also relates to electrolyte compositions and electrode materials containing such salts and to batteries containing them.
Battery electrolytes, being either liquid, gel or solid, generally consists in one or more lithium salts dissolved in a solvent and/or a solvating polymer. Additives may also further be added to improve the electrolyte's properties, e.g. its stability. Some of these salts may also be included in an electrode material to improve ionic conductivity of the material. Among the salts generally used, LiPF6 (lithium hexafluorophosphate) possesses interesting properties, but degrades in the presence of water to form hydrofluoric acid (HF). This HF formed may result in a dissolution of the cathode material.
Other salts were also developed, including LiFSI and LiTFSI as well as LiTDI. These salts also have their own drawbacks. For example, the TFSI-anion is very reactive and often leads to the corrosion of the aluminum current collector even at low voltage. Both LiFSI and LiTFSI are not recommended for high voltage applications and are expensive. LiTDI is more stable than the other two but is very hygroscopic and has conductivity and solubility issues.
Therefore, it is highly desirable to develop new salts for use in electrolyte compositions or as additives in electrode materials, for instance, having one or more of the following advantages compared to currently used salts: improved ionic conductivity, lower production costs, improved solubility in electrolyte solvents, and/or the formation of a more conductive SEI.
According to one aspect, here is described a compound, for instance a salt, for use in electrolyte compositions and/or as additive in electrode materials. In one embodiment, the compound is as defined in Formula I:
In one embodiment, R3 is NHSO2R4. In another embodiment, R3 is NHSO2OR4. For instance, R4 is a C1-6alkyl substituted with at least one of fluorine and alkoxy, or R4 is a C6aryl substituted with at least one fluorine atom. In another embodiment, R3 is a heterocycle. In another embodiment, at least one of R1 and R2 is CN, or both of R1 and R2 are CN.
In a further embodiment, the compound of Formula I is compound is selected from:
According to another embodiment, the compound is as defined in Formula II:
In one embodiment, R5 is an unsubstituted C1-6alkyl group. In another embodiment, R5 is a fluorinated C1-6alkyl group. In a further embodiment, R6 is a fluorinated C1-6alkyl group. In yet another embodiment, R6 is a fluorinated C6aryl group. In yet another embodiment, at least one of R5 and R6 is an optionally substituted C6aryl group (e.g. a C6aryl group substituted with one or more fluorine atoms). In other embodiments, the compound is of Formula II, provided that when R6 is trifluoromethyl, then R5 is other than methyl or trifluoromethyl.
In a further embodiment, the compound of Formula II is compound is selected from:
According to a further embodiment, the compound is as defined in Formula III:
In one embodiment, R7 is a fluorine atom. In another embodiment, R7 is selected from fluorine substituted C1-6alkyl groups. In a further embodiment, L1 is a covalent bond or L1 is a linker selected from optionally substituted C6aryl groups.
In a further embodiment, the compound of Formula III is compound is selected from:
According to another embodiment, the compound is as defined in Formula IV:
In one embodiment, X1 is a carbon atom. In one embodiment, R8 and R9 are different. Alternatively, R8 and R9 are the same. In another embodiment, at least one of R8 and R9 is CN or optionally substituted C1-6alkyl. In one embodiment, R8 and R9 are both CN or optionally substituted C1-6alkyl, or R8 and R9 are both CN, or R8 and R9 are both fluorine substituted C1-6alkyl. In another embodiment, X1 is a nitrogen atom. For example, X1 is a nitrogen atom and R9 is a fluorine substituted SO2Alkyl (e.g. SO2CF3). In another embodiment, m is 0. In a further embodiment m is 1.
In a further embodiment, the compound of Formula IV is compound is selected from:
According to yet another embodiment, the compound is as defined in Formula V:
In one embodiment, at least one of R1 and R2 is CN. For example, both of R1 and R2 are CN. In another embodiment, X1 is a carbon atom. For example, X1 is a carbon atom and R8 and R9 are both CN or optionally substituted C1-6alkyl, or X1 is a carbon atom and R8 and R9 are both CN, or X1 is a carbon atom and R8 and R9 are both fluorine substituted C1-6alkyl. In another embodiment, X1 is a nitrogen atom. For instance, X1 is a nitrogen atom and R9 is a fluorine substituted SO2Alkyl (e.g. SO2CF3).
In a further embodiment, the compound of Formula V is compound is selected from:
In one embodiment, described is a compound according to any one of the foregoing embodiments, wherein M is Li and n is 1. In another embodiment, the compound is as herein defined and is a di-salt (e.g. a dianion forming a salt with two alkali metal anions, where applicable). For example, the compounds of Formulae I, IV and V, the compound may include a further anion on a second nitrogen atom. For instance, Compounds E1 to E4 may form a disalt, such as, for compound E2:
Further contemplated are the free forms of any of the salts referred to herein.
According to another aspect, the present technology relates to an electrode material comprising, as an additive, a compound as herein defined, and at least one electrochemically active material.
According to another aspect, the present technology relates to an electrolyte composition comprising a compound as herein described. For instance, the electrolyte composition further comprises a compatible solvent. In another example, the electrolyte composition further comprises a compatible solvating polymer.
In a further aspect, also contemplated is an electrochemical cell comprising an electrolyte, an electrode and a counter-electrode, wherein at least one of the electrode or counter-electrode comprises an electrode material comprising, as an additive, a compound as herein defined, and at least one electrochemically active material. Alternatively, contemplated is an electrochemical cell which comprises an electrolyte composition comprising a compound as herein defined, an electrode and a counter-electrode. In one embodiment, the electrochemical cell comprises a compound as herein defined in an electrolyte composition and in at least one electrode material. In one embodiment, electrochemical cell is included in a battery, an electrochromic device, or a capacitor. For instance, the battery is a lithium or lithium-ion battery. In other examples, the battery is a sodium or potassium battery.
According to another aspect, described in the use of the electrochemical cell as herein defined in electrical or hybrid vehicles, or in ubiquitous IT devices.
Other features and advantages of the present technology will be better understood upon reading of the description herein below.
Here are described compounds (e.g. salts) intended for use as electrode material additives or as a component of an electrolyte composition. Compounds described are of one of
Formulae I to V as herein defined. Exemplary compounds are also described and should not be interpreted as limiting the scope of the broader formulae.
Accordingly, the compound may be as defined in Formula I:
For example, R3 is NHSO2R4, or R3 is NHSO2OR4. For instance, R3 is NHSO2R4 or NHSO2OR4 and R4 is a C1-6alkyl substituted with at least one of fluorine and alkoxy, or R4 is a C6aryl substituted with at least one fluorine atom. In another example, R3 is a heterocycle having 5 or 6 cycle atoms (e.g. a non-aromatic heterocycle having 5 or 6 cycle atoms linked through a nitrogen atom, such as a maleimide). In another embodiment, at least one of R1 and R2 is CN, or both of R1 and R2 are CN.
Examples of compounds of Formula I include, without limitation, Compounds A1 to A5 as defined above, or a tautomer thereof.
The compound may also be defined as in Formula II:
For example, R5 is an unsubstituted C1-6alkyl group (such as methyl, ethyl, propyl, isopropyl and the like), or R5 is a fluorinated C1-6alkyl group (e.g. trifluoromethyl, and the like). In another example, R6 is a fluorinated C1-6alkyl group (e.g. trifluoromethyl, and the like) or R6 is a fluorinated C6aryl group (e.g. pentafluorophenyl, and the like). Other examples include compounds of Formula II wherein at least one of R5 and R6 is an optionally substituted C6aryl group. In other examples, the compound is of Formula II, provided that when R6 is trifluoromethyl, then R5 is other than methyl or trifluoromethyl.
Examples of compounds of Formula II include, without limitation, Compounds B1 to B4, as herein defined, or a tautomer thereof. For instance, the compound is Compounds B3 or B4, as herein defined, or a tautomer thereof.
The compound may also be as defined in Formula III:
For example, R7 is a fluorine atom or R7 is selected from fluorine substituted C1-6alkyl groups. According to some examples, L1 is a covalent bond. According to other examples, L1 is a linker selected from optionally substituted C6aryl groups.
Examples of compounds of Formula III include, without limitation, Compounds C1 to C4, as herein defined, or a tautomer thereof.
The compound may further be defined as in Formula IV:
In some examples, X1 is a carbon atom. When X1 is a carbon atom, R8 and R9 may be the same or different. For instance, X1 is a carbon atom and at least one of R8 and R9 is CN or optionally substituted C1-6alkyl. For instance, X1 is a carbon atom and R8 and R9 are both CN or optionally substituted C1-6alkyl, or R8 and R9 are both CN, or R8 and R9 are both fluorine substituted C1-6alkyl. According to other examples, X1 is a nitrogen atom. For example, X1 is a nitrogen atom, R8 is absent and R9 is a fluorine substituted SO2Alkyl (e.g. SO2CF3). In one example, m is 0. In a further example, m is 1.
Examples of compounds of Formula IV include, without limitation, Compounds D1 to D6, as herein defined, or a tautomer thereof.
The compound may also further be defined as in Formula V:
For example, at least one of R1 and R2 is CN, or both of R1 and R2 are CN. In some examples, X1 is a carbon atom. For instance, X1 is a carbon atom and R8 and R9 are both CN or optionally substituted C1-6alkyl, or X1 is a carbon atom and R8 and R9 are both CN, or X1 is a carbon atom and R8 and R9 are both fluorine substituted C1-6alkyl. In other examples, X1 is a nitrogen atom. For instance, X1 is a nitrogen atom and R9 is a fluorine substituted SO2Alkyl (e.g. SO2CF3).
Examples of compounds of Formula V include, without limitation, Compounds E1 to E4, as herein defined, or a tautomer thereof.
According to one example, the compound is as defined in any one of Formulae I to V, wherein M is Li and n is 1. In another embodiment, the compound is as herein defined and is a di-salt (e.g. a dianion forming a salt with two alkali metal anions, where applicable). For example, the compounds of Formulae I, IV and V, the compound may include a further anion on a second nitrogen atom. Further contemplated are the free forms of any of the salts referred to herein.
As used herein, the term “alkyl” refers to saturated hydrocarbons having from one to sixteen carbon atoms, including linear or branched alkyl groups. Examples of alkyl groups include, without limitation, methyl, ethyl, propyl, butyl, pentyl, hexyl, heptyl, octyl, nonyl, decyl, isopropyl, tert-butyl, sec-butyl, isobutyl, and the like. When the alkyl group is located between two functional groups, then the term alkyl also encompasses alkylene groups such as methylene, ethylene, propylene, and the like. The term “C1-6alkyl” refers to an alkyl group having from 1 to the indicated “n” number of carbon atoms.
The term “alkoxy” as used herein means an alkyl group having an oxygen atom attached thereto. Representative alkoxy groups include groups having 1 to about 6 carbon atoms, e.g., methoxy, ethoxy, propoxy, tert-butoxy and the like. Examples of alkoxy groups include methoxy, ethoxy, isopropyloxy, propoxy, butoxy, pentoxy, fluoromethoxy, difluoromethoxy, trifluoromethoxy, chloromethoxy, dichloromethoxy, trichloromethoxy groups and the like. The term alkoxy includes both unsubstituted or substituted alkoxy groups, etc., as well as halogenated alkyloxy groups.
The term “aryl” refers to aromatic groups having 4n+2π (pi) electrons, wherein n is an integer from 1 to 3, in a conjugated monocyclic or polycyclic system (fused or not) and having six to fourteen ring atoms. A polycyclic ring system includes at least one aromatic ring. Aryl may be directly attached, or connected via a C1-C3alkyl group (also referred to as arylalkyl or aralkyl). Examples of aryl groups include, without limitation, phenyl, benzyl, phenethyl, 1-phenylethyl, tolyl, naphthyl, biphenyl, terphenyl, indenyl, benzocyclooctenyl, benzocycloheptenyl, azulenyl, acenaphthylenyl, fluorenyl, phenanthrenyl, anthracenyl, and the like. The term aryl includes both unsubstituted aryl groups and substituted aryl groups. The term “C6-Cnaryl” refers to an aryl group having from 6 to the indicated “n” number of carbons in the ring structure.
The terms “heterocycle” or “heterocyclic” include heterocycloalkyl and heteroaryl groups. Examples of heterocycles include, without limitation, acridinyl, azocinyl, benzimidazolyl, benzofuranyl, benzothiofuranyl, benzothiophenyl, benzoxazolyl, benzthiazolyl, benztriazolyl, benztetrazolyl, benzisoxazolyl, benzisothiazolyl, benzimidazolinyl, carbazolyl, 4αH-carbazolyl, carbolinyl, chromanyl, chromenyl, cinnolinyl, decahydroquinolinyl, 2H,6H-1,5,2-dithiazinyl, dihydrofuro[2,3-b]tetrahydrofuran, furanyl, furazanyl, imidazolidinyl, imidazolinyl, imidazolyl, 1H-indazolyl, indolenyl, indolinyl, indolizinyl, indolyl, 3H-indolyl, isobenzofuranyl, isochromanyl, isoindazolyl, isoindolinyl, isoindolyl, isoquinolinyl, isothiazolyl, isoxazolyl, methylenedioxyphenyl, morpholinyl, naphthyridinyl, octahydroisoquinolinyl, oxadiazolyl, 1,2,3-oxadiazolyl, 1,2,4-oxadiazolyl, 1,2,5-oxadiazolyl, 1,3,4-oxadiazolyl, oxazolidinyl, oxazolyl, oxazolidinyl, pyrimidinyl, phenanthridinyl, phenanthrolinyl, phenazinyl, phenothiazinyl, phenoxathiinyl, phenoxazinyl, phthalazinyl, piperazinyl, piperidinyl, piperidonyl, 4-piperidonyl, piperonyl, pteridinyl, purinyl, pyranyl, pyrazinyl, pyrazolidinyl, pyrazolinyl, pyrazolyl, pyridazinyl, pyridooxazole, pyridoimidazole, pyridothiazole, pyridinyl, pyridyl, pyrimidinyl, pyrrolidinyl, pyrrolinyl, 2H-pyrrolyl, pyrrolyl, quinazolinyl, quinolinyl, 4H-quinolizinyl, quinoxalinyl, quinuclidinyl, tetrahydrofuranyl, tetrahydroisoquinolinyl, tetrahydroquinolinyl, tetrazolyl, 6H-1,2,5-thiadiazinyl, 1,2,3-thiadiazolyl, 1,2,4-thiadiazolyl, 1,2,5-thiadiazolyl, 1,3,4-thiadiazolyl, thianthrenyl, thiazolyl, thienyl, thienothiazolyl, thienooxazolyl, thienoimidazolyl, thiophenyl, triazinyl, 1,2,3-triazolyl, 1,2,4-triazolyl, 1,2,5-triazolyl, 1,3,4-triazolyl, xanthenyl, and the like. The term heterocycle includes both unsubstituted heterocyclic groups and substituted heterocyclic groups.
The term “substituted”, when in association with any of the foregoing groups refers to a group substituted at one or more position with substituents such as cyano, halogen, nitro, trifluoromethyl, lower alkyl, cycloalkyl, heterocycloalkyl, aryl, heteroaryl, lower alkoxy, aryloxy, benzyloxy, benzyl, sulfonyl, sulfonate, sulfonamide, phosphonato, phosphinato, oxo, and the like. Any of the above substituents can be further substituted if permissible, e.g. if the group contains an alkyl group, an alkoxy group, or an aryl group.
Also described is an electrode material comprising, as an additive, a compound as herein defined, and at least one electrochemically active material. The electrochemically active material may be a material for use in a negative electrode. Alternatively, the electrochemically active material may be a material for use in a positive electrode. Examples of electrochemically active materials include, without limitation, titanates and lithium titanates (e.g. TiO2, Li2TiO3, Li4Ti5O12, H2Ti5O11, H2Ti4O9, or a combination thereof), lithium and metal phosphates (e.g. LiM′PO4 where M′ is Fe, Ni, Mn, Co, or a combination thereof), vanadium oxides (e.g. LiV3O8, V2O5, Li2O5, and the like), and other lithium and metal oxides such as LiMn2O4, LiM″O2 (M″ being Mn, Co, Ni, or a combination thereof), Li(NiM′″)O2 (M′″ being Mn, Co, Al, Fe, Cr, Ti, Zr, and the like, or a combination thereof), or a combination thereof. For instance, the active material is selected from Lithium iron phosphate (LFP), lithium manganese iron phosphate (LMFP), lithium titanate (LTO), graphite, and lithium nickel manganese cobalt oxide (NMC). The particles may be freshly formed or of commercial source, in the form of microparticles or nanoparticles and may further include a carbon coating.
The electrode material may also optionally include additional components like conductive materials, inorganic particles, glass or ceramic particles, and the like. Examples of conductive materials include carbon black, Ketjen™ black, acetylene black, graphite, graphene, carbon fibers, nanofibers (e.g. VGCF) or nanotubes, or a combination thereof. The electrode material may also further comprise a binder. Examples of binders include water soluble binders such as SBR (styrene butadiene rubber), NBR (butadiene acrylonitrile rubber), HNBR (hydrogenated NBR), CHR (epichlorohydrin rubber), ACM (acrylate rubber), and the like, and cellulose-based binders (e.g. carboxyalkylcellulose, hydroxyalkylcellulose, and combinations), or any combination of two or more of these. For instance, the carboxyalkylcellulose may be carboxymethylcellulose (CMC) or carboxyethylcellulose. Hydroxypropylcellulose is an example of hydroxyalkylcellulose. Other examples of binders include fluorine-containing polymeric binders such as PVDF and PTFE, and ion-conductive polymer binders such as block copolymers composed of at least one lithium-ion solvating segment and at least one cross-linkable segment.
According to another aspect, the present technology relates to an electrolyte composition comprising a compound as herein described. The electrolyte may be a liquid, gel or solid polymer electrolyte and, in the case of a lithium or lithium-ion electrochemical cell, is conductive to lithium ions. For instance, the electrolyte composition further comprises a compatible solvent. In another example, the electrolyte composition further comprises a compatible solvating polymer.
For example, electrolytes are prepared by dissolution of one or more of the present compounds in an appropriate electrolyte solvent or solvating polymer for polymer electrolyte preparation. For use in lithium and lithium ion batteries, the compounds as lithium salts can be dissolved at an appropriate concentration, for example between 0.05 and 3 mol/litre. For other types of batteries, other salts of the present compounds should be dissolved, for example, sodium salts for sodium batteries, magnesium salts for magnesium batteries, and the like.
Non-limiting examples of electrolyte solvents include organic solvents such as ethers, carbonate esters, cyclic carbonate esters, aliphatic carboxylic acid esters, aromatic carboxylic acid esters, phosphate esters, sulfite esters, nitriles, amides, alcohols, sulfoxides, sulfolane, nitromethane, 1,3-dimethyl-2-imidazolidinone, 1,3-diméthyl-3,4,5,6-tetrahydro-2(1,H)-pyrimidinone, 3-methyl-2-oxazolidinone, or a mixture thereof. In particular examples, the solvent may also be an aqueous solvent, i.e. water or a mixture comprising water.
Examples of solvents include dimethyl carbonate, diethyl carbonate, ethyl methyl carbonate, propylene carbonate, ethylene carbonate, y-butyrolactone, glyme, diglyme, triglyme, tetraglyme, sulfolane, tetraethylsulfamide, acetonitrile, pyruvonitrile, propionitrile, methoxypropionitrile, dimethylaminopropionitrile, butyronitrile, isobutyronitrile, valeronitrile, pivalonitrile, isovaléronitrile, glutaronitrile, méthoxyglutaronitrile, 2-methylglutaronitrile, 3-methylglutaronitrile, adiponitrile, malononitrile, and combinations thereof. Various additives may also be included in the electrolyte composition to improve its properties.
Non-limiting examples of polymers for use in electrolytes (e.g. gel or solid) include poly(ethylene oxide) and its copolymers and block-copolymers, poly(propylene oxide) and its copolymers and block-copolymers, poly(dimethylsiloxane) and its copolymers and block-copolymers, poly(alkylene carbonate) and their copolymers and block-copolymers, poly(alkylenesulfone) and its copolymers and block-copolymers, poly(alkylenesulfamides) and its copolymers and block-copolymers, polyurethanes and their copolymers and block-copolymers, poly(vinylalcohol) and its copolymers and block-copolymers and combinations thereof. Additionally, branched or cross-linked solvating polymers may also be included. Various additives may also be included in the polymer electrolyte composition to improve its properties.
Electrochemical cells as herein described comprise an electrolyte, an electrode and a counter-electrode, wherein at least one of the electrode or counter-electrode comprises an electrode material comprising, as an additive, a compound as herein defined, and at least one electrochemically active material as defined above. Alternatively, contemplated is an electrochemical cell which comprises an electrolyte composition comprising a compound as herein defined, an electrode and a counter-electrode. In one embodiment, the electrochemical cell comprises a compound as herein defined in an electrolyte composition and in at least one electrode material. In one embodiment, the electrochemical cell is included in a battery, an electrochromic device, or a capacitor. For instance, the battery is a lithium or lithium-ion battery. In other examples, the battery is a sodium or potassium battery.
According to another aspect, described in the use of the electrochemical cell as herein defined in electrical or hybrid vehicles, or in ubiquitous IT devices.
The following non-limiting examples are illustrative embodiments and should not be construed as further limiting the scope of the present application.
2-Amino-1H-imidazole-4,5-dicarbonitrile (1.1 eq), trifluorosulfonylchloride (1 eq), lithium carbonate (2 eq) and N′N-dimethylaminopyridine (DMAP) (0.25 eq) were introduced in a Schlenk flask. The solids were degassed by vacuum-N2 cycles. Dry acetone (1M) was added and the suspension was vigorously stirred and heated under reflux overnight. The reaction mixture was cooled down to room temperature. Distilled water was added, and the solution was extracted using dichloromethane. The combined organic layers were washed with water and acidic water, dried using MgSO4 and filtered. The solution was filtered on a diatomaceous earth filtration aid sold under the trademark CELITE® to eliminate inorganic residues. The organic solution was concentrated under reduced pressure until dryness. The solid residue was purified by silica gel chromatography using hexanes/ethyl acetate (1/1) as eluent. A crystalline yellow solid was isolated after evaporation. This yellow solid was then dissolved in water and monohydrated lithium hydroxide was added until a slight excess of base was detected using a pH paper. The solution was concentrated until dryness by reduced pressure distillation. The solid was suspended in diethyl carbonate (DEC) and stirred overnight at room temperature. The solution was passed through a diatomaceous earth filtration aid sold under the trademark CELITE® and the clear solution was concentrated under reduced pressure and dried in a vacuum oven for 24 hours.
2,4,6-Trichloro-[1,3,5]-triazine (1 eq.) was added to a room temperature solution of sulfonic acid (1 eq.) in dry acetone, followed by trimethylamine (1 eq.) dropwise. The solution was stirred vigorously and heated at 90° C. overnight. The reaction mixture was cooled to room temperature and, under nitrogen, 2-amino-1H-imidazole-4,5-dicarbonitrile (1.2 eq.), DMAP (0.25 eq.) and lithium carbonate (2 eq.) were added. The mixture was stirred vigorously and heated at 90° C. for 2 days. The reaction mixture was cooled down to room temperature. Distilled water was added, and the solution was extracted using dichloromethane. The combined organic layers were washed with water and acidic water, dried using MgSO4 and filtered. The solution was filtered on a diatomaceous earth filtration aid sold under the trademark CELITE® to eliminate inorganic residues. The organic solution was concentrated under reduced pressure until dryness. The solid residue was purified by silica gel chromatography using hexanes/ethyl acetate (1/1) as eluent. A crystalline yellow solid was isolated. The yellow solid was then dissolved in water and monohydrated lithium hydroxide was added until a slight excess of base was detected using a pH paper. The solution was concentrated until dryness by reduced pressure distillation. The solid was suspended in diethyl carbonate (DEC) and stirred overnight at room temperature. The solution was passed through a diatomaceous earth filtration aid sold under the trademark CELITE ® and the clear solution was concentrated under reduced pressure and dried in a vacuum oven for 24 hours.
2-Amino-1H-imidazole-4,5-dicarbonitrile (1.1 eq), pentafluorosulfonylchloride (1 eq), lithium carbonate (2 eq) and N′N-dimethylaminopyridine (DMAP) (0.25 eq) were introduced in a Schlenk flask. The solids were degassed by vacuum-N2 cycles. Dry acetone (1M) was added and the suspension was vigorously stirred and heated under reflux. The reaction mixture was cooled down to room temperature. Distilled water was added, and the solution was extracted using dichloromethane. The combined organic layers were washed with water and acidic water, dried using MgSO4 and filtered. The solution was filtered on a diatomaceous earth filtration aid sold under the trademark CELITE® to eliminate inorganic residues. The organic solution was concentrated under reduced pressure until dryness. The solid residue was purified by silica gel chromatography using hexanes/ethyl acetate (1/1) as eluent. A crystalline yellow solid was isolated. The yellow solid was then dissolved in water and monohydrated lithium hydroxide was added until a slight excess of base was detected using a pH paper. The solution was concentrated until dryness by reduced pressure distillation. The solid was suspended in diethyl carbonate (DEC) and stirred overnight at room temperature. The solution was passed through a diatomaceous earth filtration aid sold under the trademark CELITE® and the clear solution was concentrated under reduced pressure and dried in a vacuum oven for 24 hours.
Step 1: A solution of 2-methoxyethan-1-ol in THF was added dropwise to a solution of sulfuryl chloride (1.2 eq) in THF at −75° C. The reaction mixture was warmed up to room temperature. The solution was concentrated until dryness under reduced pressure. The colorless oil obtained was used without purification.
Step 2: 2-amino-1H-imidazole-4,5-dicarbonitrile (1.1 eq), 2-methoxyethan-1-sulfonylchloride (1 eq), lithium carbonate (2 eq) and N′N-dimethylaminopyridine (DMAP) (0.25 eq) were introduced in a Schlenk flask. The solids were degassed by vacuum-N2 cycles. Dry acetone (1M) was added and the suspension was stirred vigorously and heated under reflux overnight. The reaction mixture was cooled to room temperature. Distilled water was added and the resulting solution was extracted using dichloromethane. The organic layers were combined, washed with water and acidic water, dried on MgSO4 and filtered. The organic solution obtained was concentrated under reduced pressure until dryness. The resulting brown oil was purified by silica gel chromatography. A yellow oil was isolated. The resulting compound was converted to its lithium salt by dissolution in water and addition of lithium hydroxide. The solution was concentrated until dryness by reduced pressure distillation. The solid was suspended in diethyl carbonate (DEC) and stirred overnight at room temperature. The solution was passed through a diatomaceous earth filtration aid sold under the trademark CELITE® and the clear solution was concentrated under reduced pressure and dried in a vacuum oven for 24 hours.
2-amino-1H-imidazole-4,5-dicarbonitrile and maleic anhydride were dissolved in 1,4-dioxane. The solution was heated at 150° C. during 10 hours by microwaves activation. The mixture was precipitated in cold diethyl ether and filtrated. The yellowish filtrate was evaporated, and a pale yellow highly hydroscopic solid was isolated. The solid was then dissolved in water and monohydrated lithium hydroxide was added until a slight excess of base was detected using a pH paper. The solution was concentrated until dryness by reduced pressure distillation. The solid was suspended in diethyl carbonate (DEC) and stirred overnight at room temperature. The solution was passed through a diatomaceous earth filtration aid sold under the trademark CELITE® and the clear solution was concentrated under reduced pressure and dried in a vacuum oven for 24 hours.
Acetamide (1.1 eq), trifluorosulfonylchloride (1 eq), lithium carbonate (2 eq) and N′N-dimethylaminopyridine (DMAP) (0.25 eq) were introduced in a Schlenk flask. The solids were degassed by vacuum-N2 cycles. Dry acetone (1M) was added and the suspension was stirred vigorously and heated under reflux overnight. The reaction mixture was cooled down to room temperature. Distilled water was added, and the solution was extracted using dichloromethane. The combined organic phases were washed with water, dried on MgSO4 and filtered. The organic solution was concentrated to dryness under reduced pressure. The crude oil was then dissolved in water and monohydrated lithium hydroxide was added until a slight excess of base was detected using a pH paper. The solution was concentrated until dryness by reduced pressure distillation. The solid was suspended in diethyl carbonate (DEC) and stirred overnight at room temperature. The solution was passed through a diatomaceous earth filtration aid sold under the trademark CELITE® and the clear solution was concentrated under reduced pressure and dried in a vacuum oven for 24 hours.
Trifluorocetamide (1.1 eq), trifluorosulfonylchloride (1 eq), lithium carbonate (2 eq) and N′N-dimethylaminopyridine (DMAP) (0.25 eq) were introduced in a Schlenk flask. The solids were degassed by vacuum-N2 cycles. Dry acetone (1M) was added and the suspension was stirred vigorously and heated under reflux overnight. The reaction mixture was cooled to room temperature. Distilled water was added, and the solution was extracted using dichloromethane. The organic layers were combined, washed with water, dried on MgSO4 and filtered. The organic solution was concentrated to dryness under reduced pressure. The crude oil was then dissolved in water and monohydrated lithium hydroxide was added until a slight excess of base was detected using a pH paper. The solution was concentrated until dryness by reduced pressure distillation. The solid was suspended in diethyl carbonate (DEC) and stirred overnight at room temperature. The solution was passed through a diatomaceous earth filtration aid sold under the trademark CELITE® and the clear solution was concentrated under reduce pressure and dried in vacuum oven for 24 hours.
Acetamide (1.1 eq), pentafluorobenzenesulfonyl chloride (1 eq), lithium carbonate (2 eq) and N′N-dimethylaminopyridine (DMAP) (0.25 eq) were introduced in a Schlenk flask. The solids were degassed by vacuum-N2 cycles. Dry acetone (1M) was added and the suspension was stirred vigorously and heated under reflux overnight. The reaction mixture was cooled to room temperature, distilled water was added, and the solution was extracted using dichloromethane. The organic layers were combined, washed with water, dried on MgSO4 and filtered. The crude solid was then dissolved in water and monohydrated lithium hydroxide was added until a slight excess of base was detected using a pH paper. The solution was concentrated until dryness by reduced pressure distillation. The solid was suspended in diethyl carbonate (DEC) and stirred overnight at room temperature. The solution was passed through a diatomaceous earth filtration aid sold under the trademark CELITE® and the clear solution was concentrated under reduced pressure and dried in a vacuum oven for 24 hours.
Trifulorocetamide (1.1 eq), pentafluorobenzenesulfonyl chloride (1 eq), lithium carbonate (2 eq) and N′N-dimethylaminopyridine (DMAP) (0.25 eq) were introduced in a Schlenk flask. The solids were degassed by vacuum-N2 cycles. Dry acetone (1M) was added and the suspension was stirred vigorously and heated under reflux overnight. The reaction mixture was cooled to room temperature, distilled water was added, and the solution was extracted using dichloromethane. The organic layers were combined, washed with water, dried on MgSO4 and filtered. The crude solid was then dissolved in water and monohydrated lithium hydroxide was added until a slight excess of base was detected using a pH paper. The solution was concentrated until dryness by reduced pressure distillation. The solid was suspended in diethyl carbonate (DEC) and stirred overnight at room temperature. The solution was passed on a diatomaceous earth filtration aid sold under the trademark CELITE® and the clear solution was concentrated under reduce pressure and dried in vacuum oven for 24 hours.
Step 1: Sulfanilamide, lithium carbonate (1 eq.) and 4-nitrophenyl trifluoromethanesulfonate were mixed and ground using a mortar and pestle. The molten mixture was stirred at 180° C. for one hour under nitrogen. Deionized water was added to the hot mixture under vigorous stirring. The insoluble suspended solid was removed by filtration. Water was removed under reduced pressure. The solid was washed with cold THF, ethyl acetate and a white solid was filtered. The yellow filtrate was evaporated under reduce pressure and the yellow solid was dried overnight at 40° C. under vacuum.
Step 2: A THF solution of the solid from step 1 was added to a solution of maleic anhydride in 1,4-dioxane and the resulting mixture was stirred at room temperature for 12 hours. The corresponding carboxylic acid was isolated as a white solid by filtration and was dried under vacuum at 60° C. for 4 hours.
Step 3: A acetic anhydride solution of the carboxylic acid from step 2 and sodium acetate was heated at 70° C. for 3 hours. Then, the solution was poured into an excess of diethyl ether to complete the precipitation. The resulting precipitate was isolated by filtration and dried under vacuum at 60° C. overnight.
A solution of diaminomaleonitrile (1.0 g, 4.625 mmol) and anhydrous dimethylformamide (10 mL) is added to an inert reactor. The compound 2-[bis(methylthio)methylene]malononitrile (DM3) (0.787 g, 4.625 mmol) is added and the mixture stirred for 16 hours at 120° C. Solvents and volatile compounds are removed under vacuum. The resulting product is purified by silica-gel chromatography using a mixture of ethyl acetate and hexanes as eluent.
A solution of compound DM3 (0.500 g, 2.94 mmol) in methanol (50 mL) is inserted into an inert reactor (pressure bomb). Ammonia (0.500 g, 29.4 mmol) is added and the reaction mixture is stirred for 16 hours at 70° C. Solvent and volatile compounds are removed under vacuum. The compound obtained (DM3-NH2) is used without further purification.
A solution of compound DM3-NH2 (0.500 g, 4.63 mmol) in THF (50 mL) is introduced in an inert reactor. Oxalyl chloride (0.587 g, 4.63 mmol) is added and the reaction mixture is stirred for 16 hours at room temperature. The solvent and volatile compounds are removed under vacuum. The product is purified by recrystallization in alcohols.
A solution of diaminomaleonitrile (8.0 g, 74.0 mmol) in anhydrous tetrahydrofuran (250 mL) is introduced in an inert reactor and the solution is degassed. Phosgene (7.32 g, 74.0 mmol) is added and the mixture is stirred for 1 hour. Ethanethiol (14.9 g, 148.0 mmol) is then added and the mixture is stirred for another 16 h. The solvent and volatile compounds are removed under vacuum. Acetone (100 mL) and 5 drops of 12 M HCl are added and the mixture is heated for 16 h at 120° C. until a complete discoloration from orange to grey-white is observed. The product is a grey-white powder.
Conductivity measurements were carried out with a biologic conductivity meter (model MCS-10) using a platinum cell (type HTCC: parallel plates platinized platinum on glass holder). The salts were dried in a vacuum oven at 70° C. for one night prior to use, and PC/EMC/DMC (4/3/3) or distilled water were used as solvent. Solutions of LiCl (in water) or LiPF6 (in PC/EMC/DMC) were used as references.
Numerous modifications could be made to any of the embodiments described above without departing from the scope of the present invention. Any references, patents or scientific literature documents referred to in this application are incorporated herein by reference in their entirety for all purposes.
This application is a divisional of U.S. application Ser. No. 16/494,435, filed Sep. 16, 2019, titled “LITHIUM SALTS OF CYANO-SUBSTITUTED IMIDAZOLE FOR LITHIUM ION BATTERIES”, which is a U.S. National Phase Under U.S.C. § 371 of International Application No. PCT/CA2018/050370, titled “SALTS FOR USE IN ELECTROLYTE COMPOSITIONS OR AS ELECTRODE ADDITIVES,” filed Mar. 27, 2018, which claims priority to U.S. provisional application No. 62/477,161 filed on Mar. 27, 2017, the contents of which are incorporated herein by reference in their entirety for all purposes.
| Number | Date | Country | |
|---|---|---|---|
| 62477161 | Mar 2017 | US |
| Number | Date | Country | |
|---|---|---|---|
| Parent | 16494435 | Sep 2019 | US |
| Child | 18661081 | US |
