Polymers from stabilized imines
US-9879118-B2 · Jan 30, 2018 · US
US10113034B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-10113034-B2 |
| Application number | US-201615334156-A |
| Country | US |
| Kind code | B2 |
| Filing date | Oct 25, 2016 |
| Priority date | Oct 5, 2015 |
| Publication date | Oct 30, 2018 |
| Grant date | Oct 30, 2018 |
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The disclosure describes new compositions and methods related to polyaminals and related polymers. The compositions are useful as therapeutic/drug conjugates, self-healing materials, reversible crosslinking materials, degradable hydrogels, protective coatings, and as metal scavenging agents. New atom efficient synthetic schemes are disclosed, which yield previously unobtainable high molecular weight polyaminals.
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What is claimed is: 1. A method for producing a polymer, comprising: forming a reaction mixture comprising a non-polar solvent and an imine compound comprising electron withdrawing or accepting groups; adding a multifunctional nucleophile to the mixture; and heating the mixture at a temperature from about 50° C. to about 150° C. to produce a polymer. 2. The method of claim 1 , wherein the imine compound comprises at least two imine groups. 3. The method of claim 2 , wherein the two imine groups comprise at least one aromatic ring. 4. The method of claim 1 , wherein the imine compound comprises electron withdrawing or accepting groups selected from the group consisting of: electronegative heteroatoms, positively charged groups, quaternary amine groups, conjugated groups, aromatic groups, halogens, nitriles, carbonyls, nitro groups, nitroso groups, sulfones, and sulfonates. 5. The method of claim 1 , wherein the multifunctional nucleophile comprises at least two nucleophilic groups, wherein each nucleophilic group comprises an atom selected from the group consisting of: C, Si, Ge, Sn, N, P, As, Sb, O, S, Se, and Te. 6. The method of claim 1 , wherein the imine compound is formed by exposing an amine precursor to a formaldehyde. 7. The method of claim 2 , wherein the two imine groups are formed by exposing a diamine precursor to a formaldehyde. 8. The method of claim 1 , wherein forming the reaction mixture comprises adding an aromatic diamine and paraformaldehyde to the non-polar solvent to form the imine compound. 9. A method for producing a polymer, comprising: forming a reaction mixture comprising a non-polar solvent, a formaldehyde, and an imine precursor compound comprising electron withdrawing or accepting groups; reacting the imine precursor compound with the formaldehyde to form an imine compound; adding a multifunctional nucleophile to the mixture; and heating the mixture at a temperature from about 50° C. to about 150° C. to produce a polymer. 10. The method of claim 9 , wherein the imine compound comprises at least two imine groups. 11. The method of claim 10 , wherein the two imine groups comprise at least one aromatic ring. 12. The method of claim 9 , wherein the imine precursor compound is an aromatic diamine. 13. The method of claim 9 , wherein the multifunctional nucleophile comprises at least two nucleophilic groups, wherein each nucleophilic group comprises an atom selected from the group consisting of: C, Si, Ge, Sn, N, P, As, Sb, O, S, Se, and Te. 14. The method of claim 9 , wherein the imine precursor compound is an aminobenzene compound. 15. A method for producing a polymer, comprising: forming a reaction mixture comprising a non-polar solvent, a formaldehyde, and an aminobenzene compound; reacting the aminobenzene compound with the formaldehyde to form an imine compound; adding a multifunctional nucleophile comprising an atom selected from the group consisting of: C, Si, Ge, Sn, N, P, As, Sb, O, S, Se, and Te to the mixture; and heating the mixture at a temperature from about 50° C. to about 150° C. to produce a polymer. 16. The method of claim 15 , wherein the aminobenzene compound is a dianiline compound. 17. The method of claim 16 , wherein the aminobenzene compound comprises —CF 3 .
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