IP Library Granted Patent US 10,644,342
Granted Patent B2
US 10,644,342 · App. 15/060,493 · Granted May 5, 2020

Coordination complexes containing monosulfonated catecholate ligands and methods for producing the same

Inventors: Scott Thomas Humbarger (Cambridge, MA); Matthew Millard (Cambridge, MA)
Assignee: Lockheed Martin Energy, LLC
H01M8/188C07F7/28H01B1/121H01M8/08H01M8/20H01M10/36C07C37/00Y02E60/528
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Quick Facts
Patent No.
US 10,644,342
App. No.
15/060,493
Granted
May 5, 2020
Kind
B2
Abstract

Flow batteries and other electrochemical systems can contain an active material that is a coordination complex having at least one monosulfonated catecholate ligand or a salt thereof bound to a metal center. The monosulfonated catecholate ligand has a structure of More particularly, the coordination complex can be a titanium coordination complex with a formula of D g Ti(L 1 )(L 2 )(L 3 ), in which D is a counterion selected from H, NH 4 + , Li + , Na + , K + , or any combination thereof g ranges between 3 and 6; and L 1 , L 2 and L 3 are ligands, where at least one of L 1 , L 2 and L 3 is a monosulfonated catecholate ligand. Methods for synthesizing such monosulfonated catecholate ligands can include providing a neat mixture of catechol and up to about 1.3 stoichiometric equivalents of sulfuric acid, and heating the neat mixture at a temperature of about 80° C. or above to form 3,4-dihydroxybenzenesulfonic acid or a salt thereof.

Claims (18)

1. A method comprising heating a neat mixture of catechol and a sub-stoichiometric amount of sulfuric acid at a temperature in a range of from about 80° C. to about 130° C. to form a reaction product comprising unreacted catechol and 3,4-dihydroxybenzenesulfonic acid.

2. The method of claim 1 , wherein the reaction product comprises less than about 5% of 2,3-dihydroxybenzenesulfonic acid.

3. The method of claim 1 , wherein the neat mixture contains between about 0.2 and 0.4 stoichiometric equivalents of sulfuric acid per catechol.

4. The method of claim 3 , wherein the reaction product is a mixture of unreacted catechol and 3,4-dihydroxybenzenesulfonic acid in a molar ratio of 2:1.

5. The method of claim 4 , further comprising treating the reaction product with a base to form a desired salt form of the reaction product before further using the reaction mixture.

6. The method of claim 5 , further comprising reacting the salt form of the reaction product with a transition metal compound to form a transition metal coordination complex having one sulfonated catecholate ligand and two unsubstituted catecholate ligands bound to a metal center, wherein the sulfonated catechol ligand is a salt form of 3,4-dihydroxybenzenesulfonic acid.

7. The method of claim 6 , wherein the transition metal compound is a titanium compound.

8. The method of claim 5 , wherein the base comprises an alkali metal hydroxide, alkali metal carbonate, alkali metal bicarbonate, ammonium hydroxide, ammonium carbonate, or ammonium bicarbonate.

9. The method of claim 5 , wherein the base is lithium hydroxide, sodium hydroxide, potassium hydroxide, or a mixture thereof.

10. The method of claim 4 , wherein the reaction product is reacted with a transition metal compound to form a transition metal coordination complex having one sulfonated catecholate ligand and two unsubstituted catecholate ligands bound to a metal center, and wherein the sulfonated catechol ligand is a salt form of 3,4-dihydroxybenzenesulfonic acid.

11. The method of claim 10 , wherein the transition metal compound is a titanium compound.

12. The method of claim 1 , wherein the neat mixture contains between about 0.3 and about 0.5 stoichiometric equivalents of sulfuric acid per catechol.

13. The method of claim 12 , wherein the neat mixture contains about 0.5 stoichiometric equivalents of sulfuric acid per catechol, resulting in a reaction product that is a mixture of unreacted catechol and 3,4-dihydroxybenzenesulfonic acid in a molar ratio of 1:1, the method further comprising treating the reaction product with a base to form a desired salt form before further using the reaction mixture.

14. The method of claim 13 , wherein the base comprises an alkali metal hydroxide, alkali metal carbonate, alkali metal bicarbonate, ammonium hydroxide, ammonium carbonate, or ammonium bicarbonate.

15. The method of claim 13 , wherein the base is lithium hydroxide, sodium hydroxide, potassium hydroxide, or a mixture thereof.

16. The method of claim 13 , further comprising reacting the salt form of the reaction product with a transition metal compound to form a transition metal coordination complex having one sulfonated catecholate ligand and one unsubstituted catecholate ligand bound to a metal center, wherein the sulfonated catechol ligand is a salt form of 3,4-dihydroxybenzenesulfonic acid.

17. The method of claim 1 , wherein the neat mixture is heated at a temperature ranging between about 80° C. and about 110° C.

18. The method of claim 1 , wherein the neat mixture is heated at a temperature ranging between about 80° C. and about 100° C.

Assignments (3)
CORRECTIVE ASSIGNMENT TO CORRECT THE APPLICATION NO. 15397071 TO THE CORRECT NO. 15297071 PREVIOUSLY RECORDED ON REEL 045349 FRAME 0108. ASSIGNOR(S) HEREBY CONFIRMS THE CHANGE OF NAME. Recorded Mar 29, 2018
From: LOCKHEED MARTIN ADVANCED ENERGY STORAGE, LLC
To: LOCKHEED MARTIN ENERGY, LLC
Reel/Frame 046933/0775 →
CHANGE OF NAME Recorded Feb 15, 2018
From: LOCKHEED MARTIN ADVANCED ENERGY STORAGE, LLC
To: LOCKHEED MARTIN ENERGY, LLC
Reel/Frame 045349/0108 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 4, 2016
From: HUMBARGER, SCOTT THOMAS; MILLARD, MATTHEW
To: LOCKHEED MARTIN ADVANCED ENERGY STORAGE, LLC
Reel/Frame 038008/0693 →
Continuity (1)
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