Click chemistry as a means to functionalize macroporous PolyHIPE

D.M. Cummins, C.J. Duxbury, P.J.L.M. Quaedflieg, P.C.M.M. Magusin, C.E. Koning, A. Heise

Research output: Contribution to journalArticleAcademicpeer-review

47 Citations (Scopus)

Abstract

The surface functionalization of macroporous polyHIPE (pHIPE) was achieved by Huisgen-type 'click' chemistry. In the first step a 600-800 nm thick layer of poly(glycidyl methacrylate) (pGMA) was grafted from the pHIPE surface by atom transfer radical polymerization (ATRP). Near quantitative azidation of the pGMA layer was achieved by the ring-opening reaction of the epoxide groups with sodium azide. The influence of the reaction conditions on the uniformity of the 'click' reaction on the three-dimensional macroporous materials was shown in model reactions with propargyl alcohol. Under optimized conditions, azide conversions of around 80% were estimated from IR-spectra. Visualization of the homogeneous functionalization was achieved by the attachment of a fluorescent molecule. Moreover, the first proof of the versatility for biofunctionalization of pHIPE by this method was provided by the attachment of several protected amino acids. The hydrolytic stability of the triazole ring allows for the successful deprotection of the amino acids on the pHIPE. © 2009 The Royal Society of Chemistry.
Original languageEnglish
Pages (from-to)804-811
JournalSoft Matter
Volume5
Issue number4
DOIs
Publication statusPublished - 2009

Fingerprint Dive into the research topics of 'Click chemistry as a means to functionalize macroporous PolyHIPE'. Together they form a unique fingerprint.

Cite this