Thiocarbonyl-based poly(O-thiocarbamate) compound and preparation method and use thereof
US-12351687-B2 · Jul 8, 2025 · US
US9988495B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9988495-B2 |
| Application number | US-201615081810-A |
| Country | US |
| Kind code | B2 |
| Filing date | Mar 25, 2016 |
| Priority date | Jan 22, 2016 |
| Publication date | Jun 5, 2018 |
| Grant date | Jun 5, 2018 |
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An oligomer additive is provided. The oligomer additive is obtained by a reaction of a maleimide, a barbituric acid and a dibenzyl trithiocarbonate. A lithium battery including an anode, a cathode, a separator, an electrolyte solution and a package structure is also provided, wherein the cathode includes the oligomer additive.
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What is claimed is: 1. An oligomer additive is obtained by a reaction of a maleimide, a barbituric acid and a dibenzyl trithiocarbonate. 2. The oligomer additive according to claim 1 , wherein a molar ratio of the maleimide to the barbituric acid is between 1:1 and 4:1. 3. The oligomer additive according to claim 1 , wherein a usage amount of the maleimide is 70.8 parts by weight to 90.6 parts by weight, a usage amount of the barbituric acid is 29.2 parts by weight to 9.4 parts by weight, and a usage amount of the dibenzyl trithiocarbonate is 1 part by weight to 10 parts by weight, based on 100 parts by weight of a total weight of the maleimide and the barbituric acid. 4. The oligomer additive according to claim 1 , wherein the maleimide comprises a mono-maleimide or a bismaleimide, wherein the mono-maleimide is selected from the group consisting of N-phenylmaleimide, N-(o-methylphenyl)-maleimide, N-(m-methylphenyl)-maleimide, N-(p-methylphenyl)-maleimide, N-cyclohexylmaleimide, maleimidophenol, maleimidobenzocyclobutene, phosphorus-containing maleimide, phosphonate-containing maleimide, siloxane-containing maleimide, N-(4-tetrahydropyranyl-oxyphenyl)maleimide, and 2,6-xylylmaleimide, and the bismaleimide has a structure represented by formula 1: wherein R 1 comprises: 5. The oligomer additive according to claim 1 , wherein the barbituric acid has a structure represented by formula 2: wherein R 2 and R 3 are each independently selected from the group consisting of —H, —CH 3 , —C 2 H 5 , —C 6 H 5 , —CH(CH 3 ) 2 , —CH 2 CH(CH 3 ) 2 , —CH 2 CH 2 CH(CH 3 ) 2 , and 6. A lithium battery, comprising: an anode; a cathode configured separately from the anode, wherein the cathode comprises the oligomer additive according to claim 1 ; a separator disposed between the anode and the cathode, wherein the separator, the anode, and the cathode define a housing region; an electrolyte solution disposed in the housing region; and a package structure packaging the anode, the cathode, and the electrolyte solution. 7. The lithium battery according to claim 6 , wherein the electrolyte solution comprises an organic solvent, a lithium salt, and an additive. 8. The lithium battery according to claim 7 , wherein the additive comprises mono-maleimide, polymaleimide, bismaleimide, polybismaleimide, a copolymer of bismaleimide and mono-maleimide, vinylene carbonate, or a mixture thereof.
Li-accumulators · CPC title
Polythiocarbonates · CPC title
Rocking-chair batteries, i.e. batteries with lithium insertion or intercalation in both electrodes; Lithium-ion batteries · CPC title
characterised by the additives · CPC title
Macromolecular compounds obtained by reactions forming a linkage containing nitrogen with or without oxygen or carbon in the main chain of the macromolecule, not provided for in groups C08G12/00 - C08G71/00 {(polycarbodiimides prepared from isocyanates C08G18/025, C08G18/797)} · CPC title
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