Author:

Keywords:

porous polymer, surface functionalized, click chemistry, 13C NMR, Science & Technology, Physical Sciences, Technology, Chemistry, Physical, Materials Science, Multidisciplinary, Physics, Multidisciplinary, Polymer Science, Chemistry, Materials Science, Physics, SELF-ASSEMBLED MONOLAYERS, SOLUBLE POROGENIC SOLVENTS, UBER DIE POLYMERISATION, PHASE EMULSIONS HIPES, IN-OIL EMULSIONS, SURFACE-AREA, UMGEKEHRTER EMULSION, POROUS POLYMERS, AMINO-ACIDS, FOAMS, 02 Physical Sciences, 03 Chemical Sciences, 09 Engineering, Chemical Physics, 34 Chemical sciences, 40 Engineering, 51 Physical sciences

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.