IP Library Granted Patent US 11,981,777
Granted Patent B2
US 11,981,777 · App. 16/545,470 · Granted May 14, 2024

Synthesis of hyperbranched polymethacrylates and polyacrylates by a haloinimer approach

Inventors: Coleen Pugh (Akron, OH); Chenwei Liu (Patchogue, NY); Cesar Lopez Gonzalez (Akron, OH); Chenying Zhao (Houston, TX)
Assignee: The University of Akron
C08G83/005A61L15/24A61L15/64A61L26/0014A61L26/009C07K1/145C08F20/68C09D135/02
View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 11,981,777
App. No.
16/545,470
Granted
May 14, 2024
Kind
B2
Abstract

A new synthetic pathway for hyperbranched polyacrylates and polymethacrylates including the steps of preparing an inimer and polymerizing the inimer to form hyperbranched polymers or copolymers.

Claims (42)

1. A method for preparing hyperbranched polyacrylates or polymethacrylates, the method comprising:

(a) reacting a halohydrin containing a carboxylic acid group with an acrylic anhydride or methacrylic anhydride in the presence of p-toluenesulfonic acid (pTsOH) as an acid catalyst, to form a pre-inimer that contains a carboxylic acid group, wherein the step of reacting a halohydrin containing a carboxylic acid group with an acrylic anhydride or methacrylic anhydride comprises the following reaction:

wherein R is methyl and wherein X is bromine or chlorine;

(b) reacting the pre-inimer with a chlorinating agent to form an acid chloride;

(c) reacting the acid chloride with an alcohol in the presence of trimethylamine to esterify the acid chloride and form an inimer, wherein the step of reacting the acid chloride with an alcohol comprises the following reaction:

wherein R is methyl, wherein X is bromine or chlorine, and wherein R 1 is selected from aliphatic, non-aliphatic, fluorocarbon, monosaccharides, disaccharides, polysaccharides, cyclodextrins in deprotected form or protected form with acetate, isopropylidene, silyl ether, ketal or chloroacetate protecting groups, protected amines, sulfates, sulfonates, acids, thiols, ionomer species, linear or branched, mesogenic chiral, achiral, hydrocarbon, non-hydrocarbon, fluorocarbon, oligo(oxyethylene), siloxane, mesogenic group, non-mesogenic groups, aliphatic, non-aliphatic, perfluoro alkyl, and perfluoroaryl groups; and

(d) polymerizing the inimer to form a hyperbranched polyacrylate or polymethacrylate polymer by self-condensing vinyl polymerization, or copolymerizing the inimer with one or more monomers using self-condensing vinyl co-polymerization.

2. The method of claim 1 , wherein the halohydrin containing a carboxylic acid group is prepared by a process comprising the following reaction:

wherein R is methyl and wherein X is bromine or chlorine.

3. A method for preparing hyperbranched polyacrylates or polymethacrylates, the method comprising:

(a) reacting a halohydrin containing a carboxylic acid group with an acrylic anhydride or methacrylic anhydride in the presence of p-toluenesulfonic acid (p-TsOH), to form a pre-inimer that contains a carboxylic acid group;

(b) reacting the pre-inimer with a chlorinating agent to form an acid chloride;

(c) reacting the acid chloride with an alcohol in the presence of trimethylamine to esterify the acid chloride and form an inimer; and

(d) polymerizing the inimer to form a hyperbranched polyacrylate or polymethacrylate polymer by self-condensing vinyl polymerization, or copolymerizing the inimer with one or more monomers using self-condensing vinyl co-polymerization;

wherein the halohydrin containing a carboxylic acid group is prepared by a process comprising the following reaction:

wherein R is hydrogen or methyl and wherein X is bromine or chlorine.

4. A method for preparing hyperbranched polyacrylates or polymethacrylates, the method comprising:

(a) reacting a halohydrin containing a carboxylic acid group with an acrylic anhydride or methacrylic anhydride in the presence of p-toluenesulfonic acid (p-TsOH), to form a pre-inimer that contains a carboxylic acid group;

(b) reacting the pre-inimer with a chlorinating agent to form an acid chloride;

(c) reacting the acid chloride with an alcohol in the presence of trimethylamine to esterify the acid chloride and form an inimer; and

(d) polymerizing the inimer to form a hyperbranched polyacrylate or polymethacrylate polymer by self-condensing vinyl polymerization, or copolymerizing the inimer with one or more monomers using self-condensing vinyl co-polymerization;

wherein the halohydrin containing a carboxylic acid group is prepared by a process comprising the following reaction:

wherein R is hydrogen or methyl, le is methyl, ethyl, isopropyl, terbutyl, or diphenyl, and X is bromine or chlorine.

5. A method for preparing hyperbranched polyacrylates or polymethacrylates, the method comprising:

(a) reacting a halohydrin containing a carboxylic acid group with an acrylic anhydride or methacrylic anhydride in the presence of p-toluenesulfonic acid (pTsOH) as an acid catalyst, to form a pre-inimer that contains a carboxylic acid group, wherein the step of reacting a halohydrin containing a carboxylic acid group with an acrylic anhydride or methacrylic anhydride comprises the following reaction:

wherein R is methyl and wherein X is bromine or chlorine;

(b) reacting the pre-inimer with an alcohol using carbodiimide coupling or a Mitsunobu reaction to form an ester inimer; and

(c) polymerizing the ester inimer to form a hyperbranched polyacrylate or polymethacrylate polymer by self-condensing vinyl polymerization, or copolymerizing the ester inimer with one or more monomers using self-condensing vinyl co-polymerization.

6. The method of claim 5 , wherein the step of reacting the pre-inimer with an alcohol comprises the following reaction:

wherein R is methyl, wherein X is bromine or chlorine, and wherein R 1 is selected from aliphatic, non-aliphatic, fluorocarbon, monosaccharides, disaccharides, polysaccharides, cyclodextrins in deprotected form or protected form with acetate, isopropylidene, silyl ether, ketal or chloroacetate protecting groups, protected amines, sulfates, sulfonates, acids, thiols, ionomer species, linear or branched, mesogenic chiral, achiral, hydrocarbon, non-hydrocarbon, fluorocarbon, oligo(oxyethylene), siloxane, mesogenic group, non-mesogenic groups, aliphatic, non-aliphatic, perfluoro alkyl, and perfluoroaryl groups.

7. The method of claim 5 , wherein the step of reacting the pre-inimer with an alcohol comprises the following reaction:

wherein R is methyl, wherein X is bromine or chlorine, and wherein R 1 is selected from aliphatic, non-aliphatic, fluorocarbon, monosaccharides, disaccharides, polysaccharides, cyclodextrins in deprotected form or protected form with acetate, isopropylidene, silyl ether, ketal or chloroacetate protecting groups, protected amines, sulfates, sulfonates, acids, thiols, ionomer species, linear or branched, mesogenic chiral, achiral, hydrocarbon, non-hydrocarbon, fluorocarbon, oligo(oxyethylene), siloxane, mesogenic group, non-mesogenic groups, aliphatic, non-aliphatic, perfluoro alkyl, and perfluoroaryl groups.

8. A method for preparing hyperbranched polyacrylates or polymethacrylates, the method comprising:

(a) reacting a halohydrin containing a carboxylic acid group with an acrylic anhydride or methacrylic anhydride in the presence of p-toluenesulfonic acid (p-TsOH), to form a pre-inimer that contains a carboxylic acid group;

(b) reacting the pre-inimer with an alcohol using carbodiimide coupling or a Mitsunobu reaction to form an ester inimer; and

(c) polymerizing the ester inimer to form a hyperbranched polyacrylate or polymethacrylate polymer by self-condensing vinyl polymerization;

wherein the step of polymerizing the ester inimer comprises either reaction a below or reaction b below:

9. A method for preparing hyperbranched polyacrylates or polymethacrylates, the method comprising:

(a) reacting a halohydrin containing a carboxylic acid group with an acrylic anhydride or methacrylic anhydride in the presence of p-toluenesulfonic acid (p-TsOH), to form a pre-inimer that contains a carboxylic acid group;

(b) reacting the pre-inimer with an alcohol using carbodiimide coupling or a Mitsunobu reaction to form an ester inimer; and

(c) copolymerizing the ester inimer with one or more monomers using self-condensing vinyl co-polymerization;

wherein the step of copolymerizing the ester inimer comprises the following reaction:

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 9, 2020
From: PUGH, COLEEN; LIU, CHENWEI; GONZALEZ, CESAR LOPEZ; ZHAO, CHENYING
To: THE UNIVERSITY OF AKRON
Reel/Frame 051532/0162 →
CONFIRMATORY LICENSE Recorded Oct 28, 2019
From: UNIVERSITY OF AKRON
To: NATIONAL SCIENCE FOUNDATION
Reel/Frame 050841/0900 →
Continuity (2)
Provisional Application 62719880 · Aug 20, 2018
Related Publication 20200055995A1 · Feb 20, 2020