“…[4] In particular,thiol-ene [5][6][7] and thiol-yne [8] reactions have been employed in photopolymerizations.T hey proceed by as tep-growth mechanism involving the radical propagation by addition of photogenerated thiyl radicals-using atype Ior type II photoinitiator-onto av inyl monomer,f ollowed by achain-transfer reaction (Figure 1). Thiol-ene reactions have for example recently been used for the synthesis of hydrogels, [9][10][11][12] bioorganic-functionalized materials, [13,14] polymerdispersed liquid-crystalline phases, [15,16] 3D-printing, [17][18][19] telechelic polyethylenes, [20] etc. However,i ft hiol-ene and -yne reactions have been adopted by many academics,t hiols often smell bad, and are generally too unstable for industrial applications,inparticular in (meth)acrylate formulations because of the competitive Michael addition.…”