Issue 11, 2014

Highly tunable polyurethanes: organocatalyzed polyaddition and subsequent post-polymerization modification of pentafluorophenyl ester sidechains

Abstract

A facile method for the synthesis of high molecular weight functionalized polyurethanes from a novel pentafluorophenyl ester-containing diol precursor is described. Specifically, polyurethanes containing the activated ester sidechains were synthesized via triflic acid-catalyzed polyaddition of the above diol with diisocyanates. This was followed by quantitative postpolymerization modification of the sidechains with various primary amines. This method represents an efficient and modular synthetic strategy for the preparation of functionalized polyurethanes.

Graphical abstract: Highly tunable polyurethanes: organocatalyzed polyaddition and subsequent post-polymerization modification of pentafluorophenyl ester sidechains

Supplementary files

Article information

Article type
Communication
Submitted
20 Feb 2014
Accepted
13 Mar 2014
First published
14 Mar 2014

Polym. Chem., 2014,5, 3547-3550

Highly tunable polyurethanes: organocatalyzed polyaddition and subsequent post-polymerization modification of pentafluorophenyl ester sidechains

H. Sardon, J. M. W. Chan, R. J. Ono, D. Mecerreyes and J. L. Hedrick, Polym. Chem., 2014, 5, 3547 DOI: 10.1039/C4PY00262H

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