Method and Composition For Reducing Nitrates, Nitrites, and/or Hydroxylamine in Water Using a Homogeneous Reduced Copper Tetra-Substituted Fluorinated Pinacolate Ligand Catalyst Complex

Abstract

A method for reducing nitrates, nitrites, and/or hydroxylamine in water using a homogeneous reduced copper tetra-substituted fluorinated pinacolate ligand catalyst complex. The method includes dissolving a copper(II) tetra-substituted fluorinated pinacolate ligand pre-catalyst complex in water having an excess amount of nitrates, nitrites, and/or hydroxylamine therein. The dissolved copper(II) tetra-substituted fluorinated pinacolate ligand pre-catalyst complex in the water is subjected to electrochemical reduction to form a homogeneous reduced copper tetra-substituted fluorinated pinacolate ligand catalyst complex. The homogeneous reduced copper tetra-substituted fluorinated pinacolate ligand catalyst complex reduces the nitrates, nitrites, and/or hydroxylamine in the water to compounds with nitrogen in a lower oxidation state with the homogeneous reduced copper tetra-substituted fluorinated pinacolate ligand catalyst complex.

Claims

1. A method for reducing nitrates, nitrites, and/or hydroxylamine in water using a homogeneous reduced copper tetra-substituted fluorinated pinacolate ligand catalyst complex, the method comprising: dissolving a copper(II) tetra-substituted fluorinated pinacolate ligand pre-catalyst complex in water having an excess amount of nitrates, nitrites, and/or hydroxylamine therein; subjecting the dissolved copper(II) tetra-substituted fluorinated pinacolate ligand pre-catalyst complex in the water to electrochemical reduction to form a homogeneous reduced copper tetra-substituted fluorinated pinacolate ligand catalyst complex; and reducing the nitrates, nitrites, and/or hydroxylamine in the water to compounds with nitrogen in a lower oxidation state with the homogeneous reduced copper tetra-substituted fluorinated pinacolate ligand catalyst complex.

2. The method of claim 1 in which the copper(II) tetra-substituted fluorinated pinacolate ligand pre-catalyst complex includes substituents configured as fluorinated aryl groups or fluorinated alkyl groups.

3. The method of claim 1 in which the copper(II) tetra-substituted fluorinated pinacolate ligand pre-catalyst complex includes at least one fluorinated aryl group and a remainder of groups including fluorinated aryl groups or fluorinated alkyl groups.

4. The method of claim 3 further including providing a nucleophilic tether including a hydrocarbon linker and a nucleophilic group configured to couple the homogeneous reduced copper tetra-substituted fluorinated pinacolate ligand catalyst complex copper(II) to a surface with the tetra-substituted fluorinated pinacolate ligand pre-catalyst complex.

5. The method of claim 4 in which the nucleophilic tether includes an alkyl chain with nucleophilic group.

6. The method of claim 5 in which the nucleophilic tether includes a propyl amino group.

7. The method of claim 4 in which the surface includes one or more of: silicon dioxide (SiO.sub.2), fluorinated tin oxide (FTO), and indium-doped tin oxide (ITO).

8. The method of claim 3 in which the homogeneous copper(II) tetra-substituted fluorinated pinacolate ligand pre-catalyst complex includes copper(II) mono{di(pentaflurophenyl)di(trifluromethyl)} pinacolate.

9. The method of claim 3 in which the copper(II) tetra-substituted fluorinated pinacolate ligand pre-catalyst complex includes copper(II) bis{di(pentaflurophenyl)di(trifluromethyl)} pinacolate.

10. The method of claim 1 in which the copper(II) tetra-substituted fluorinated pinacolate ligand pre-catalyst complex includes copper(II) bis(perfluoropinacolate).

11. The method of claim 1 further including providing a buffer to control the pH of the water and the homogeneous reduced copper tetra-substituted fluorinated pinacolate ligand catalyst complex to a pH in the range of about 8 to 11.

12. The method of claim 1 in which the electrochemical reduction includes applying an electrical potential between an anode and a cathode placed in the water having the copper(II) tetra-substituted fluorinated pinacolate ligand pre-catalyst complex therein at a potential in the range of about −0.95 V to about −1.20 V.

13. The method of claim 4 in which surface includes the surface of a flow tube configured to receive a flow of the water having an excess amount of the nitrates, nitrites, and/or hydroxylamine.

14. The method of claim 13 in which the homogeneous reduced copper tetra-substituted fluorinated pinacolate ligand catalyst complex including at least one fluorinated aryl coupled to the surface of the flow tube is configured to reduce the nitrates, nitrites, and and/or hydroxylamine in the flow of the water to the compounds with nitrogen in a lower oxidation state.

15. The method of claim 13 in which the homogeneous reduced copper tetra-substituted fluorinated pinacolate ligand catalyst complex including at least one fluorinated aryl coupled to the surface of the flow tube is configured to remove the nitrates, nitrites, and and/or hydroxylamine in the flow of the water to the compounds with nitrogen in a lower oxidation state.

16. The method of claim 14 in which the water having excess nitrates, nitrites, and/or hydroxylamine therein includes water from a municipal water supply.

17. A method for tethering a tetra-substituted fluorinated pinacolate ligand to a surface, the method comprising: providing a nucleophilic tether configured to couple to the surface the nucleophilic tether including a hydrocarbon linker and a nucleophilic group; and reacting the nucleophilic group with a tetra-substituted fluorinated pinacol to bond the nucleophilic group to the tetra-substituted fluorinated pinacol and form a tethered tetra-substituted fluorinated pinacol; deprotonating the tethered tetra-substituted fluorinated pinacol with a base to form a tethered tetra-substituted fluorinated pinacolate; and complexing copper to the tethered tetra-substituted fluorinated pinacolate to form a tethered copper tetra-substituted fluorinated pinacolate ligand pre-catalyst complex.

18. The method of claim 17 in which the tetra-substituted fluorinated pinacol includes at least one fluorinated aryl group and a remainder of groups including fluorinated aryl groups or fluorinated alkyl groups.

19. The method of claim 18 in which the tetra-substituted fluorinated pinacol includes di(pentaflurophenyl)di(trifluromethyl)} pinacol.

20. The method of claim 17 in which the tethered copper tetra-substituted fluorinated pinacolate ligand catalyst complex includes at least one fluorinated aryl group and a remainder of groups including fluorinated aryl groups or fluorinated alkyl groups.

21. The method of claim 17 in which the tethered homogeneous copper(II) tetra-substituted fluorinated pinacolate ligand pre-catalyst complex is configured as copper(II) mono{di(pentaflurophenyl)di(trifluromethyl)} pinacolate ligand pre-catalyst complex.

22. The method of claim 17 in which the tethered copper(II) tetra-substituted fluorinated pinacolate ligand pre-catalyst complex is configured as copper(II) bis{di-pentaflurophenyl di-tri fluromethyl} pinacolate ligand pre-catalyst complex.

23. The method of claim 17 in which the nucleophilic tether includes an alkyl chain with nucleophilic group.

24. The method of claim 23 in which the nucleophilic tether includes propyl amino.

25. The method of claim 17 in which the surface includes one or more of: silicon dioxide (SiO.sub.2), fluorinated tin oxide (FTO), and indium doped tin oxide (ITO).

26. A copper(II) tetra-substituted fluorinated pinacolate ligand pre-catalyst complex for reducing nitrates, nitrites, and/or hydroxylamine in water, the copper(II) tetra-substituted fluorinated pinacolate ligand pre-complex comprising: a copper(II) tetra-substituted fluorinated pinacolate ligand pre-catalyst complex including: at least one fluorinated aryl group and; a remainder of groups including fluorinated aryl groups or fluorinated alkyl groups.

27. The copper(II) tetra-substituted fluorinated pinacolate ligand pre-catalyst complex of claim 26 in which the fluorinated aryl group includes pentafluorophenyl group.

28. The copper(II) tetra-substituted fluorinated pinacolate ligand pre-catalyst complex of claim 26 in which the fluorinated alkyl groups include trifluoromethyl.

29. The homogeneous copper tetra-substituted fluorinated pinacolate ligand pre-catalyst complex of claim 26 in which the copper(II) tetra-substituted fluorinated pinacolate ligand pre-catalyst complex is configured as copper(II) mono{di(pentaflurophenyl)di(trifluromethyl)} pinacolate ligand pre-catalyst complex.

30. The copper(II) tetra-substituted fluorinated pinacolate ligand pre-catalyst complex of claim 26 in which the copper(II) tetra-substituted fluorinated pinacolate ligand pre-catalyst is configured as copper(II) bis{di(pentaflurophenyl)di(trifluromethyl)} pinacolate ligand pre-catalyst complex.

31. A tetra-substituted fluorinated pinacolate ligand pre-catalyst complex tethered to a surface comprising: a nucleophilic tether including a hydrocarbon linker and a nucleophilic group coupled the surface; and a copper(II) tetra-substituted fluorinated pinacolate ligand pre-catalyst complex coupled to the nucleophilic tether.

32. The tetra-substituted fluorinated pinacolate ligand pre-catalyst complex tethered to the surface of claim 31 in which the copper(II) tetra-substituted fluorinated pinacolate ligand pre-catalyst complex includes at least one fluorinated aryl group and a remainder of groups including fluorinated aryl groups or fluorinated alkyl groups.

33. The tetra-substituted fluorinated pinacolate ligand pre-catalyst complex tethered to the surface of claim 31 in which the copper(II) tetra-substituted fluorinated pinacolate ligand pre-catalyst complex is configured as copper(II) mono{di(pentaflurophenyl)di(trifluromethyl)} pinacolate ligand pre-catalyst complex.

34. The tetra-substituted fluorinated pinacolate ligand pre-catalyst complex tethered to the surface of claim 31 in which the copper(II) tetra-substituted fluorinated pinacolate ligand pre-catalyst complex is configured as copper(II) bis{di-pentaflurophenyl di-tri fluromethyl} pinacolate ligand pre-catalyst complex.

35. The tetra-substituted fluorinated pinacolate ligand pre-catalyst complex tethered to the surface of claim 31 in which the nucleophilic tether includes an alkyl chain with nucleophilic group.

36. The tetra-substituted fluorinated pinacolate ligand pre-catalyst complex tethered to the surface of claim 31 in which the hydrocarbon linker includes propyl amino.

37. The tetra-substituted fluorinated pinacolate ligand pre-catalyst complex tethered to the surface of claim 31 in which the surface includes one or more of: silicon dioxide (SiO.sub.2), fluorinated tin oxide (FTO), and indium doped tin oxide (ITO).

Description

BRIEF DESCRIPTION OF THE SEVERAL VIEWS OF THE DRAWINGS

[0015] Other objects, features and advantages will occur to those skilled in the art from the following description of a preferred embodiment and the accompanying drawings, in which:

[0016] FIG. 1 is a flow chart showing one example of the primary steps of one embodiment of the method of reducing nitrates, nitrites, and/or hydroxylamine in water using a homogeneous reduced copper tetra-substituted fluorinated pinacolate ligand catalyst complex of this invention;

[0017] FIG. 2 is a chemical diagram of one example of a copper(II) tetra-substituted fluorinated pinacolate ligand pre-catalyst complex of FIG. 1 in which the substituents may be fluorinated alkyl groups and fluorinated aryl groups;

[0018] FIG. 3 is a chemical diagram of copper(II) tetra-substituted fluorinated pinacolate ligand pre-catalyst complex shown in FIGS. 1 and 2 configured as a Cu (II) bis(perfluoropinacolate) ligand pre-catalyst complex;

[0019] FIG. 4 is an Oak Ridge Thermal Ellipsoid Plot (ORTEP) of the Cu (II) bis(perfluoropinacolate) ligand pre-catalyst complex shown in FIG. 3;

[0020] FIG. 5 is a schematic block diagram showing one example of the primary components which may be used by the method shown in FIG. 1;

[0021] FIG. 6 is a plot showing an example of the cathodic current increasing as the concentration of the homogeneous copper bis(perfluoropinacolate) ligand pre-catalyst complex increases in accordance with the method shown in one or more of FIGS. 1-5;

[0022] FIG. 7 is a plot showing one example of the cathodic current increasing as the concentration of nitrates increase in accordance with the method shown in one or more of FIGS. 1-5; and

[0023] FIG. 8 is a chemical diagram of one example of a copper(II) tetra-substituted fluorinated pinacolate ligand pre-catalyst complex of another embodiment of this invention including at least one substituted fluorinated aryl group and the remainder of groups including fluorinated alkyl groups or fluorinated aryl groups;

[0024] FIG. 9 is a schematic block diagram showing one example of a nucleophilic tether configured to couple the homogeneous reduced copper tetra-substituted fluorinated pinacolate ligand catalyst complex including at least one fluorinated aryl group to a surface;

[0025] FIG. 10 is a schematic block diagram showing one example of the nucleophilic tether shown in FIG. 9;

[0026] FIG. 11 is a chemical diagram of one example of the copper(II) tetra-substituted fluorinated pinacolate ligand pre-catalyst complex shown in FIG. 8 configured as copper(II) mono{di(pentaflurophenyl)di(trifluromethyl)} pinacolate;

[0027] FIG. 12 is a chemical diagram showing another embodiment of the copper(II) tetra-substituted fluorinated pinacolate ligand pre-catalyst complex shown in FIG. 8 configured as copper(II) bis{di(pentaflurophenyl)di(trifluromethyl)} pinacolate ligand pre-catalyst complex;

[0028] FIG. 13 is a schematic block diagram showing one example of a homogeneous reduced copper tetra-substituted fluorinated pinacolate ligand catalyst complex which may be coupled to the surface of the flow tube using the nucleophilic tether shown in FIGS. 9 and 10;

[0029] FIG. 14 is a flowchart showing one embodiment of the primary steps of the method for tethering a tetra-substituted fluorinated pinacolate ligand catalyst complex to a surface of this invention;

[0030] FIG. 15 is a chemical diagram showing one example of the tetra-substituted fluorinated pinacol including at least one fluorinated aryl group and a remainder of groups including fluorinated aryl groups or fluorinated alkyl groups for the method shown in FIG. 14;

[0031] FIG. 16 is a chemical diagram showing one example of a tethered tetra-substituted fluorinated pinacol shown in FIG. 15 including at least one fluorinated aryl group and a remainder of groups including fluorinated aryl groups or fluorinated alkyl groups;

[0032] FIG. 17 is a chemical diagram showing one example of the tetra-substituted fluorinated pinacol shown in FIG. 16 configured as di(pentaflurophenyl)di(trifluromethyl)} pinacol;

[0033] FIG. 18 is a chemical diagram showing one example of a tethered tetra-substituted fluorinated pinacolate including at least one fluorinated aryl group and a remainder of groups including fluorinated aryl groups or fluorinated alkyl groups;

[0034] FIG. 19 is a chemical diagram showing one example of a copper(II) tetra-substituted fluorinated pinacolate ligand pre-catalyst complex including at least one fluorinated aryl group and a remainder of groups including fluorinated aryl groups or fluorinated alkyl groups;

[0035] FIG. 20 is a chemical diagram showing of one example of a tethered copper(II) tetra-substituted fluorinated pinacolate ligand pre-catalyst complex configured as mono{di(pentaflurophenyl)di(trifluromethyl)} pinacolate ligand pre-catalyst complex;

[0036] FIG. 21 is a chemical diagram of one example of a tethered copper(II) tetra-substituted fluorinated pinacolate ligand pre-catalyst complex configured as bis{di-pentaflurophenyl di-tri fluromethyl} pinacolate ligand pre-catalyst complex; and

[0037] FIG. 22 is a schematic flowchart showing in further detail the primary steps of one embodiment of the method for tethering a tetra-substituted fluorinated pinacolate ligand to a surface shown in one or more of FIGS. 14-21.

DETAILED DESCRIPTION OF THE INVENTION

[0038] Aside from the preferred embodiment or embodiments disclosed below, this invention is capable of other embodiments and of being practiced or being carried out in various ways. Thus, it is to be understood that the invention is not limited in its application to the details of construction and the arrangements of components set forth in the following description or illustrated in the drawings. If only one embodiment is described herein, the claims hereof are not to be limited to that embodiment. Moreover, the claims hereof are not to be read restrictively unless there is clear and convincing evidence manifesting a certain exclusion, restriction, or disclaimer.

[0039] There is shown in FIG. 1 one example of the method for reducing nitrates, nitrites, and/or hydroxylamine in water using a homogeneous reduced copper tetra-substituted fluorinated pinacolate ligand catalyst complex of one embodiment of this invention. The method includes dissolving a copper(II) tetra-substituted fluorinated pinacolate ligand pre-catalyst complex in water having an excess amount of nitrates, nitrites, and/or hydroxylamine therein, step 10. In one example, copper(II) tetra-substituted fluorinated pinacolate ligand pre-catalyst complex 12, FIG. 2, may include substituents R-14 configured as fluorinated alkyl group 16, e.g., a tri-fluoromethyl (CF.sub.3) group or a perfluoroalkyl (CF.sub.2).sub.nF group, where n≧1 or as fluorinated aryl group 18, e.g., a pentafluorophenyl (C.sub.6F.sub.5) group or a perfluorobenzyl (CF.sub.2C.sub.6F.sub.5) group.

[0040] In one example, copper(II) tetra-substituted fluorinated pinacolate ligand pre-catalyst complex 12 may be configured or substituted as Cu(II) bis(perfluoropinacolate) ligand pre-catalyst complex 20, FIG. 3. FIG. 4 shows an Oak Ridge Thermal Ellipsoid Plot (ORTEP) of Cu (II) bis(perfluoropinacolate) ligand pre-catalyst complex 20. In this example, copper (II) bis(perfluoropinacolate) ligand pre-catalyst complex 20, FIG. 3, also referred to herein as [Cu(pinF).sup.2] or Cu-pinF, has 12 fluorine (F) atoms on it and zero hydrogen (H) atoms. In other examples, the copper (II) bis(fluoropinacolate) pre-catalyst ligand may have any formulation in which the total number of fluorine atoms and hydrogen atoms is 12, e.g., 10 F, 2H; 8F, 4H, and the like. Preferably, the Cu (II) bis(fluoropinacolate) ligand pre-catalyst complex is oxidation resistant.

[0041] In one example, copper (II) bis(perfluoropinacolate) ligand pre-catalyst complex may be formulated in accordance with the following example:

Example

[0042] K.sub.2[Cu(pin.sup.F).sub.2], 6.4H.sub.2O. In air, Cu(NO.sub.3).sub.2.3H.sub.2O (0.122 g, 0.501 mmol dissolved in 2 mL of H.sub.2O) was added to H.sub.2pin.sup.F (0.348 g, 1.01 mmol) dissolved in 3 mL of MeOH while stirring. Addition of an aqueous solution of KOH (0.080 g, 2.00 mmol) afforded a deep blue solution. The reaction mixture was allowed to stir for 1 h, and was then concentrated by heating at 50-60° C. Deep blue crystals were isolated after cooling down the solution to 5° C., and were washed further with a minimum amount of cold H.sub.2O and dried in air with a yield of 67% (0.295 g). Blue-colored crystals suitable for X-ray analysis were grown by slow evaporation of an aqueous solution. UV-vis (CH.sub.3CN) (λ.sub.max (ε, cm.sup.−1 M.sup.−1)): 195 (2960), 242 (6670), 646 (32); (H.sub.2O) (λ.sub.max nm (ε, cm.sup.−1 M.sup.−1)), 193 (7920), 241 (6150), 668 (22). Anal. Calcd. for C.sub.12H.sub.4 CuF.sub.24K.sub.2O.sub.6: C, 17.12; H, 0.48; F, 54.16. Found: C, 16.86; H, 0.27; F, 53.09. (Fluorine analysis likely low due to incomplete combustion) μeff (CD.sub.3CN)=1.71μ.sub.B.

[0043] The molecular structure of [Cu(pin.sup.F).sub.2].sup.2, 20, FIG. 3, as well as the solid state X-ray structure with two potassium cations, FIG. 4, have been previously published, (See, e.g., Tahsini et.al, Inorganic Chemistry, 2013, 52, 14050), incorporated by reference herein. The synthesis of homogeneous Cu bis(perfluoropinacolate) pre-catalyst complex has been established and optimized and can be done in air and using water as a solvent. The homogeneous Cu bis(perfluoropinacolate) pre-catalyst complex can be synthesized on a gram scale and may also be scaled to larger quantities. Pure material can be isolated within twenty-four hours after the start of synthesis.

[0044] The solution containing the dissolved copper(II) tetra-substituted fluorinated pinacolate ligand pre-catalyst complex is then subjected to electrochemical reduction to form a homogeneous reduced copper tetra-substituted fluorinated pinacolate ligand catalyst complex, step 22, FIG. 1. In one example, the copper(II) tetra-substituted fluorinated pinacolate ligand pre-catalyst complex may include homogeneous reduced copper bis(perfluoropinacolate) ligand catalyst complex created from copper (II) bis(perfluoropinacolate) ligand pre-catalyst complex 20, FIG. 3. In other examples, homogeneous reduced copper tetra-substituted fluorinated pinacolate ligand catalyst complex may have any formulation in which the total number of fluorine atoms and hydrogen atoms is 12, e.g., 10 F, 2H; 8F, 4H, and the like. The homogeneous reduced copper tetra-substituted fluorinated pinacolate ligand catalyst complex has an oxidation state less than Cu (II), e.g., Cu(I), Cu(0), and the like.

[0045] The homogeneous reduced copper tetra-substituted fluorinated pinacolate ligand catalyst complex reduces the nitrates, nitrites, and/or hydroxylamine in the water to compounds with nitrogen in a lower oxidation state, step 24, FIG. 1, by transferring electrons from the homogeneous reduced copper tetra-substituted fluorinated pinacolate ligand catalyst complex to nitrates, nitrites, and/or hydroxylamine. For example, nitrates, e.g., LiNO.sub.3, NaNO.sub.3, KNO.sub.3 (found in fertilizer), Ca(NO.sub.3).sub.2 with a nitrogen oxidation state of +5 may be reduced to nitrites, e.g., NaNO.sub.2 or KNO.sub.2 having a nitrogen oxidation state of +3. The nitrites may then be reduced to nitric oxide (NO) gas with an oxidation state of +2 or preferably to nitrogen gas, N.sub.2(g), with a nitrogen oxidation state of 0. Hydroxylamine, NH.sub.2OH, with a nitrogen oxidation state of −2 may be reduced to ammonia, NH.sub.3, with a nitrogen oxidation state of −3.

[0046] FIG. 5 shows one example of the primary components which may be used for subjecting copper(II) tetra-substituted fluorinated pinacolate ligand pre-catalyst complex 20 to electrochemical reduction in accordance with the method shown in FIG. 1. In this example, Cu (II) bis(perfluoropinacolate) ligand pre-catalyst complex 20 in solid form is dissolved in water 26 having an excess amount of nitrates, nitrites, and/or hydroxylamines therein. The homogeneous reduced Cu bis(perfluoropinacolate) ligand catalyst complex is then formed, exemplary indicated at 28 in water 26. In one example, the method was performed in water 26 with a KCl supporting electrolyte and a K.sub.2pin.sup.F buffer comprised of H.sub.2pin.sup.F and KOH. Preferably, the buffer may be used to control the pH of the solution of water 26 and the homogeneous reduced copper tetra-substituted fluorinated pinacolate ligand catalyst complex in water 24, e.g., homogeneous reduced Cu bis(perfluoropinacolate) ligand catalyst complex indicated at 28, to a pH in the range of about 8-11, as nitrate reduction is observed in this range, close to the pH range of tap water (6.5-8.5). An electrical potential is applied between anode 30 and cathode 32 to subject copper(II) tetra-substituted fluorinated pinacolate ligand pre-catalyst complex in water 26 to electrochemical reduction to form the homogeneous reduced copper tetra-substituted fluorinated pinacolate ligand catalyst complex, e.g., homogeneous reduced Cu bis(perfluoropinacolate) ligand complex indicated at 28, as known by those skilled in the art. Reference electrode 34 is used for reference potential. In one example, a glassy carbon or graphite working electrode (cathode 32) may be used with a platinum wire as a counter electrode (anode 30). In one example, reference electrode 34 may be Ag/AgCl. Preferably the reducing potential to generate catalytic current provided at cathode 32 in the range of about −0.95 V to about −1.2 V, e.g., about −1.0 V when compared to the reference electrode 34. A voltage closer to zero means less energy is used by the method disclosed herein.

[0047] Graph 40, FIG. 6 shows one example of the increase in the observed catalytic current as the concentration of the homogeneous Cu bis(perfluoropinacolate) ligand pre-catalyst complex 20 is increased. Graph 42, FIG. 7, shows a strong correlation of the observed concentration of NO.sub.3.sup.− and the catalytic current. In this example, the catalytic current increases proportional to the addition of NO.sub.3.sup.− because the process is NO.sub.3.sup.− dependent.

[0048] The result is a method for reducing nitrates, nitrites, and/or hydroxylamine in water using a homogeneous reduced copper tetra-substituted fluorinated pinacolate ligand catalyst complex of one or more embodiments of this invention that effectively and efficiently reduces nitrates, nitrites and/or hydroxylamines to compounds with nitrogen in a lower oxidation state. Thus, the method can reduce nitrates in water to nitrites which can then be reduced to presumed nitrogen gas to effectively and efficiently reduce and ultimately remove nitrates and/or nitrites from water. Hydroxylamines in water can also be reduced to ammonia.

[0049] The homogeneous reduced copper tetra-substituted fluorinated pinacolate ligand catalyst complex discussed above performs homogeneous catalysis, meaning that the reduction process is solution based and not a result of deposition onto the electrode. A homogeneous reduced copper tetra-substituted fluorinated pinacolate ligand catalyst complex is unique because it can reduce nitrates, nitrites and/or hydroxylamines in aqueous solution. The method for reducing nitrates, nitrites, and/or hydroxylamine in water using a homogeneous reduced copper tetra-substituted fluorinated pinacolate ligand catalyst complex performs the reduction at a lower potential, e.g., about −1.0V, when compared to conventional methods and is therefore a more efficient catalyst.

[0050] The inventors hereof realized that when the copper(II) tetra-substituted fluorinated pinacolate ligand pre-catalyst complex is configured as homogeneous reduced copper bis(fluoropincolate) ligand catalyst complex, it cannot easily be modified to put a tether on it for coupling it to a surface because of the hybridization of the carbon in the trifluoromethyl (CF.sub.3) group. To overcome this problem, the method shown in FIG. 1 further includes providing a copper(II) tetra-substituted fluorinated pinacolate ligand pre-catalyst complex 12′, FIG. 8, which includes at least one fluorinated aryl group R′-44, e.g.,

a pentafluorophenyl (C.sub.6F.sub.5) group or a perfluorobenzyl (CF.sub.2C.sub.6F.sub.5) group and the remainder of groups R-14 including fluorinated alkyl groups 16, e.g., a tri-fluoromethyl (CF.sub.3) group or a perfluoroalkyl (CF.sub.2).sub.nF group, where n≧1 or fluorinated aryl groups 18, e.g., pentafluorophenyl (C.sub.6F.sub.5) group or a perfluorobenzyl (CF.sub.2C.sub.6F.sub.5) group. The method further includes providing nucleophilic tether 50, FIG. 9, which includes hydrocarbon linker 52 and nucleophilic group 54 configured to couple homogeneous reduced copper tetra-substituted fluorinated pincolate ligand catalyst complex to a surface, e.g., surface 56, with the copper(II) tetra-substituted fluorinated pinacolate ligand pre-catalyst complex 12′, FIG. 8, which includes at least one fluorinated aryl group R′-44. In one example, nucleophilic tether 50, FIG. 9, includes an alkyl chain in a nucleophilic group as shown. In one design, nucleophilic tether 50, FIG. 10, may include propyl amino 58. Surface 56 may include one or more of silicon dioxide (SiO.sub.2), fluorinated tin oxide (FTO) or indium doped tin oxide (ITO), as shown in FIG. 10, or similar type surface.

[0051] In one example, copper(II) tetra-substituted fluorinated pincolate ligand pre-catalyst complex 12′, FIG. 8, may be configured as copper(II) mono{di(pentaflurophenyl)di(trifluromethyl)} pinacolate ligand pre-catalyst complex-60, FIG. 11. In other examples, copper(II) tetra-substituted fluorinated pinacolate ligand pre-catalyst complex-12′, FIG. 8, may be configured as copper(II) bis{di(pentaflurophenyl)di(trifluromethyl)} pinacolate ligand pre-catalyst complex-62, FIG. 12.

[0052] In one example, surface 56, FIGS. 9 and 10, may include the surface of a flow tube, e.g., surface 70, FIG. 13 of flow tube 72, configured to receive a flow of the water 74 having an excess amount of the nitrates, nitrites, and/or hydroxylamine therein. In this example, the homogeneous reduced copper tetra-substituted fluorinated pinacolate ligand catalyst complex derived from subjecting copper(II) tetra-substituted fluorinated pinacolate ligand pre-catalyst complex shown in FIG. 8, 11, or 12, subjected to electrochemical reduction discussed above is coupled to surface 70 of flow tube 72 and therefore is configured to reduce the nitrates, nitrites, and and/or hydroxylamine from flow of the water 74 to compounds with nitrogen in a lower oxidation state, as discussed above. The result is a flow of water 76 exiting flow tube 72 that may have nitrates, nitrites and/or hydroxylamines removed therefrom. In one example, flow of water 74 may be from a municipal water supply. Thus, the method for reducing nitrates, nitrites, and/or hydroxylamine in water using a homogeneous reduced copper tetra-substituted fluorinated pinacolate ligand catalyst complex may be used as an effective water treatment for removing nitrates and nitrites from water supplies, such as a municipal water supply.

[0053] FIG. 14 shows one example of the method for tethering a tetra-substituted fluorinated pincolate ligand to a surface of one embodiment of this invention. The method includes providing a nucleophilic tether configured to couple to a surface, step 80. The nucleophilic tether preferably includes a hydrocarbon linker and a nucleophilic group, e.g., nucleophilic tether 50, FIGS. 9 and 10, with hydrocarbon linker 52 and nucleophilic group 54, as discussed above. Nucleophilic group 54 is then reacted with tetra-substituted fluorinated pinacol 84, FIG. 15, to bond nucleophilic group 54, FIGS. 9 and 10, to tetra-substituted fluorinated pinacol 84 to form tethered tetra-substituted fluorinated pinacol 86, FIG. 16, step 88, FIG. 14. In one example, tetra-substituted fluorinated pinacol 84, FIG. 15, include at least one fluorinated aryl group R′-90, e.g., a pentafluorophenyl (C.sub.6F.sub.5) group, and tethered tetra-substituted fluorinated pinacol 86, FIG. 16, include at least one fluorinated aryl group R′-90, e.g., a tetrafluorophenylene, (C.sub.6F.sub.4) group. Each of tetra-substituted fluorinated pinacol 84 and tethered substituted fluorinated pinacol 86 include a remainder of groups R-92 including fluorinated alkyl groups 94, e.g. a tri-fluoromethyl (CF.sub.3) group or a perfluoroalkyl (CF.sub.2).sub.nF group, where n≧1 or fluorinated aryl groups 96 e.g., pentafluorophenyl (C.sub.6F.sub.5) group or a perfluorobenzyl (CF.sub.2C.sub.6F.sub.5) group.

[0054] Exemplary bonding of nucleophilic group 54, FIG. 16, to fluorinated aryl group R′-90 of tethered tetra-substituted fluorinated pinacol 84 is shown in captions 87 and 89. See also FIG. 22.

[0055] In one example, tetra-substituted fluorinated pinacol 84 may include di(pentaflurophenyl)di(trifluromethyl)} pinacol-98, FIG. 17.

[0056] Tethered tetra-substituted fluorinated pinacol 86, FIG. 16, is then deprotonated with a base to form tethered tetra-substituted fluorinated pincolate 99, FIG. 18, step 100, FIG. 14. Exemplary bonding of nucleophilic group 54, FIG. 18, to fluorinated aryl group R′-90 of tethered tetra-substituted fluorinated pinacolate 99 is shown in captions 103 and 105. See also FIG. 22

[0057] Copper (Cu) is then complexed to tethered tetra-substituted fluorinated pincolate 99, FIG. 18, to form tethered copper tetra-substituted fluorinated pincolate ligand pre-catalyst complex 102, FIG. 19, step 104, FIG. 14. In one design, tethered copper tetra-substituted fluorinated pincolate ligand pre-catalyst complex 102, FIG. 18 includes at least one fluorinated aryl group R′-90, e.g., C.sub.6F.sub.4 (tetrafluorophenylene) and a remainder of groups R-92 including fluorinated alkyl groups 94, e.g., a tri-fluoromethyl (CF.sub.3) group or a perfluoroalkyl (CF.sub.2).sub.nF group, where n≧1 or fluorinated aryl groups 96, e.g., pentafluorophenyl (C.sub.6F.sub.5) group or a perfluorobenzyl (CF.sub.2C.sub.6F.sub.5) group. Exemplary bonding of nucleophilic group 54 to fluorinated aryl group R′-90 of copper complexed to tetra-substituted fluorinated pinacolate 102 is shown in captions 105 and 107, similar as discussed above.

[0058] In one example, tethered homogeneous copper(II) tetra-substituted fluorinated pinacolate ligand pre-catalyst complex 102, FIG. 19, may be configured as substituted mono{di(pentaflurophenyl)di(trifluromethyl)} pinacolate ligand pre-catalyst complex-106, FIG. 20. See also FIG. 22

[0059] In another example, copper(II) tetra-substituted fluorinated pinacolate ligand pre-catalyst complex 102, FIG. 19, may be configured as substituted bis{di-pentaflurophenyl di-tri fluromethyl} pinacolate ligand pre-catalyst complex-108, FIG. 21. See also FIG. 22

[0060] Similarly, as discussed above, nucleophilic tether 50 shown in one or more of FIGS. 15, and 17-20 preferably includes alkyl chain 52, FIGS. 8 and 9, with nucleophilic group 54 and surface 56 includes one or more of silicon dioxide (SiO.sub.2), fluorinated tin oxide (FTO), or indium doped tin oxide (ITO) as discussed above, FIGS. 8 and 9.

Example

[0061] Perfluoroacetophenone is dissolved in isopropanol with a few drops of concentrated hydrochloric acid and the solution is stirred for several days while being irradiated with light from a mercury (Hg) lamp to make a yellow solution. Perfluoro(2,3-diphenyl-butane-2,3-diol) is isolated and treated with a stoichiometric amount of potassium hydroxide and copper(II) nitrate trihydrate to make a light blue solid product.

[0062] Photoreductive coupling of perfluoroacetophenone: a solution of perfluoroacetophenone (497 mg, 1.88 mmol) in isopropanol (5.0 mL) was treated with a few drops of concentrated hydrochloric acid. The stirred colorless solution was irradiated with a Hg lamp for 4 days, resulting in a clear, pale yellow solution. After concentrating in vacuo, perfluoro(2,3-diphenyl-butane-2,3-diol) was isolated from an orange oil.

[0063] Polymerization of 3-aminopropyl triethoxysilane: a solution of 3-aminopropyltriethoxysilane (APTES) (4.73 g, 21.4 mmol) in methanol (20 mL) was treated with a solution of concentrated hydrochloric acid (HCl) (6.75 mL) in methanol (20 mL) and allowed to stir for 3 weeks at room temperature to precipitate poly(APTES) as a white solid (0.959 g).

[0064] Tethering of perfluoro(2,3-diphenyl-butane-2,3-diol) to surface: a yellow stirred solution of perfluoro(2,3-diphenyl-butane-2,3-diol) (194 mg, 0.366 mmol) in isopropanol (4.0 mL) is added to a suspension of poly(APTES) in isopropanol and stirred for several days at room temperature to produce tethered-perfluoro(2,3-diphenyl-butane-2,3-diol).

[0065] Complexation of perfluoro(2,3-diphenyl-butane-2,3-diol) with copper: a yellow stirred solution of perfluoro(2,3-diphenyl-butane-2,3-diol) (194 mg, 0.366 mmol) in isopropanol (4.0 mL) was treated with a solution of potassium hydroxide (41 mg, 0.73 mmol) in isopropanol. There was no color change but the reaction mixture became cloudy. Water was added until the suspension became a solution. The clear yellow solution was added to a blue stirred solution of copper(II) nitrate trihydrate (44 mg, 0.18 mmol) in isopropanol (2.0 mL). The reaction changed color from a blue solution to a cloudy light blue suspension. After stirring for 1 h, the product was filtered to recover a light blue solid. See FIG. 21.

[0066] In addition, any amendment presented during the prosecution of the patent application for this patent is not a disclaimer of any claim element presented in the application as filed: those skilled in the art cannot reasonably be expected to draft a claim that would literally encompass all possible equivalents, many equivalents will be unforeseeable at the time of the amendment and are beyond a fair interpretation of what is to be surrendered (if anything), the rationale underlying the amendment may bear no more than a tangential relation to many equivalents, and/or there are many other reasons the applicant cannot be expected to describe certain insubstantial substitutes for any claim element amended.