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Issue 21, 2014
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Chemical functionalization of emulsion-templated porous polymers by thiol–ene “click” chemistry

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Abstract

Highly porous polymers (polyHIPEs) have been prepared by the photopolymerization of high internal phase emulsions (HIPEs) with varying ratios of thiol and acrylate monomers. The resulting polymers have a nominal porosity of 80%, and are seen to have a well-defined, interconnected pore morphology, with average pore diameters ranging from 30 to 60 μm. The polyHIPE polymers have been shown using a colourimetric (Ellman's) assay to contain residual thiols which are reactive towards a range of (meth)acrylates (hexafluoroisopropyl acrylate, fluorescein O-acrylate and poly(ethylene glycol) methyl ether methacrylate). Functionalization was explored using thermally- and UV-initiated radical-mediated “click” reactions and an amine-catalysed Michael addition reaction. The extent of functionalization was investigated qualitatively and quantitatively using a range of techniques (solid state NMR spectroscopy; FTIR spectroscopy; X-ray photoelectron spectroscopy (XPS); observation of fluorescence); high levels of conversion (up to 90–95%) were observed for the thermally-initiated radical reaction and the Michael reaction.

Graphical abstract: Chemical functionalization of emulsion-templated porous polymers by thiol–ene “click” chemistry

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Publication details

The article was received on 21 May 2014, accepted on 14 Jul 2014 and first published on 15 Jul 2014


Article type: Paper
DOI: 10.1039/C4PY00713A
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Citation: Polym. Chem., 2014,5, 6200-6206
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    Chemical functionalization of emulsion-templated porous polymers by thiol–ene “click” chemistry

    C. R. Langford, D. W. Johnson and N. R. Cameron, Polym. Chem., 2014, 5, 6200
    DOI: 10.1039/C4PY00713A

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