At Ghent University (Belgium), a new type of so-called click chemistry has been introduced. Like with most of click chemistry, it is based on a long-known efficient chemical reaction, which was now also found to be very practical for diverse and demanding applications. In particular, the unique reactivity of the studied 1,2,4-triazoline-3,5-dione (TAD) reagents has been harnessed to reversibly crosslink polyurethanes, or almost any other polymer matrix. At higher temperatures the TAD-induced crosslinks can temporarily open up, giving the thermoset the ability to be reshaped or even extruded like a typical thermoplastic polymer. This is reported in the current issue of Nature Chemistry, in a joint paper by three Ghent research groups led by Filip Du Prez, Veronique Van Speybroeck and Johan Winne. The TAD reagents used in these new click reactions are quite stable compounds in bulk, but react almost instantaneously with electron rich unsaturated organic compounds. These preferred and orthogonal reaction partners can be easily implemented in polymer chains, resulting in very straightforward macromolecular linking and functionalisation. The TAD-reagents can be clicked to these reaction partners at room temperature without the aid of any catalyst in an almost instantaneous and air- and moisture insensitive manner. In most cases, … Continue reading
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