IP Library Granted Patent US 8,378,041
Granted Patent B2
US 8,378,041 · App. 12/363,343 · Granted Feb 19, 2013

Method of preparing a star polymer macromonomer

Inventors: Jeremiah Johnson (Los Angeles, CA); Jeffrey T. Koberstein (Storrs, CT); Nicholas J. Turro (Tenafly, NJ)
Assignee: The Trustees of Columbia University in the City of New York
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 8,378,041
App. No.
12/363,343
Granted
Feb 19, 2013
Kind
B2
Abstract

The present invention relates to methods for preparing degradable model networks from any monomer functionality with any degradation methodology. It is based on the use of Atom-Transfer Radical Polymerization CLICK chemistry and a tetrafunctional initiator having terminal halogen groups to form the desired product.

Claims (8)

1. A method of preparing a star polymer macromonomer, comprising:

a) preparing a tetrafunctional initiator having terminal halogen groups, wherein the initiator contains a degradable linker for each of the terminal halogen groups, the degradable linker selected from the group consisting of a photodegradable linker, an ozonolyzable linker, and a biodegradable linker;

b) using the tetrafunctional initiator, polymerizing a first monomer through ATRP to form a polymeric halide having the terminal halogen groups;

c) modifying the polymeric halide through a post-polymerization transformation to replace the terminal halogen groups with desired functional end groups, wherein the desired functional end groups are selected from the group consisting of hydroxyl, acrylate, and azide.

2. The method of claim 1 , wherein the monomer is selected from the group consisting of acrylates, methacrylates, styrenics, and polyacids.

3. The method of claim 1 , wherein the polymerization step is repeated using a second monomer.

4. The method of claim 1 , wherein the post-polymerization transformation to add an azide functional end group comprises treating the polymeric halide with sodium azide in dimethylformamide.

5. The method of claim 1 , wherein the post-polymerization transformation is conducted to add an azide functional end group, further comprising the step of modifying the polymeric azide through CLICK chemistry to add a functional end group selected from the group consisting of aldehyde, hydroxy, carboxy, amine, peptide, epoxide, and thiol.

Assignments (2)
CONFIRMATORY LICENSE Recorded May 17, 2010
From: COLUMBIA UNIVERSITY NEW YORK MORNINGSIDE
To: NATIONAL SCIENCE FOUNDATION
Reel/Frame 024391/0521 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 19, 2009
From: JOHNSON, JEREMIAH; KOBERSTEIN, JEFFREY T.; TURRO, NICHOLAS J.
To: THE TRUSTEES OF COLUMBIA UNIVERSITY IN THE CITY OF NEW YORK
Reel/Frame 022858/0677 →
Continuity (3)
Continuation PCTUS2006041270 · Oct 24, 2006
Provisional Application 60834501 · Aug 1, 2006
Related Publication 20090259016A1 · Oct 15, 2009