Ring-opening polymerizations using a flow reactor
US-2020010610-A1 · Jan 9, 2020 · US
US11518849B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-11518849-B2 |
| Application number | US-202016882028-A |
| Country | US |
| Kind code | B2 |
| Filing date | May 22, 2020 |
| Priority date | May 22, 2020 |
| Publication date | Dec 6, 2022 |
| Grant date | Dec 6, 2022 |
A practical reading order for non-experts. Skip the full description unless you need deep technical detail.
What the patent document calls the invention.
A short plain-language summary of the technical disclosure.
Who owns or filed the patent and who is credited as inventor.
Filing, priority, publication, and grant dates set the timeline.
The legal scope of protection — read this for what is actually claimed.
Technology tags used to group this patent with similar filings.
Prior art links and similar publications in this corpus.
Official abstract text for this publication.
Techniques regarding post polymerization modifications to polycarbonate polymers via a flow reactor are provided. For example, one or more embodiments described herein can comprise a cyclic carbonate monomer that can be employed to facilitate polymerization of one or more polycarbonate platforms susceptible to post polymerization modification. For instance, one or more embodiments can regard a cyclic carbonate molecular backbone covalently bonded to an aryl halide functional group via in accordance with a chemical structure selected from the group consisting of:In the chemical structures, “R1” can be selected from the group consisting of a hydrogen atom and a functional group comprising a first alkyl group; “L” can represent a linkage group, comprising: a second alkyl group and an end group having at least one member selected from the group consisting of an oxygen atom and a nitrogen atom; and “A” can represent the aryl halide functional group.
Opening claim text (preview).
What is claimed is: 1. A monomer, comprising: a cyclic carbonate molecular backbone covalently bonded to an aryl halide functional group in accordance with a chemical structure selected from a first group consisting of: wherein R 1 is selected from a second group consisting of a hydrogen atom and a first alkyl group; wherein A is the aryl halide functional group, and has a structure selected from a third group consisting of: wherein X is a halide atom; wherein Y is an atom selected from a fourth group consisting of an oxygen atom, a nitrogen atom, and a sulfur atom; and wherein n is an integer greater than or equal to 2 and less than or equal to 8. 2. The monomer of claim 1 , wherein the first alkyl group comprises greater than or equal to one carbon atom and less than or equal to three carbon atoms. 3. The monomer of claim 1 , wherein X is the halide atom of fluorine. 4. The monomer of claim 1 , wherein the cyclic carbonate molecular backbone is covalently bonded to the aryl halide functional group in accordance with chemical structure: 5. The monomer of claim 1 , wherein the cyclic carbonate molecular backbone is covalently bonded to the aryl halide functional group in accordance with chemical structure: 6. A monomer, comprising: a cyclic carbonate molecular backbone covalently bonded to an aryl halide functional group in accordance with chemical structure: wherein R 1 is selected from a first group consisting of a hydrogen atom and a first alkyl group; wherein L is an alkylene group with an end group selected from O or NH, wherein the end group is linked to A; and wherein A is the aryl halide functional group, and has a structure selected from a second group consisting of: wherein X is a halide atom; wherein Y is an atom selected from a third group consisting of an oxygen atom, a nitrogen atom, and a sulfur atom; and wherein n is an integer greater than or equal to 2 and less than or equal to 8. 7. The monomer of claim 6 , wherein the first alkyl group comprises greater than or equal to one carbon atom and less than or equal to three carbon atoms, and wherein the alkylene group comprises greater than or equal to one carbon atom and less than or equal to twenty carbon atoms. 8. The monomer of claim 6 , wherein X is the halide atom of fluorine. 9. The monomer of claim 6 , wherein X is the halide atom of chlorine. 10. The monomer of claim 6 , wherein X is the halide atom of bromine. 11. The monomer of claim 6 , wherein X is the halide atom of iodine. 12. The monomer of claim 6 , with the chemical structure comprising: 13. The monomer of claim 6 , with the chemical structure comprising: 14. The monomer of claim 6 , with the chemical structure comprising: 15. The monomer of claim 6 , with the chemical structure comprising: 16. The monomer of claim 6 , with the chemical structure comprising: 17. The monomer of claim 6 , with the chemical structure comprising: 18. The monomer of claim 1 , wherein X is the halide atom of chlorine. 19. The monomer of claim 1 , wherein X is the halide atom of bromine. 20. The monomer of claim 1 , wherein X is the halide atom of iodine.
Microreactors placed in series, on the same or on different supports · CPC title
containing halogens · CPC title
using carbonates · CPC title
containing sulfur · CPC title
Spiral-shaped · CPC title
Related publications grouped by family.
Answers are generated from the same data shown on this page.