Thiol‐ene emulsion step polymerization in a photochemical stirred tank reactor: Molecular weight, cyclization, and fragmentation

Abstract Unlike many step polymerizations, the polymerization of bifunctional thiol and alkene monomers can be carried in emulsion to prepare a range of sulfur‐containing polymer particles differing markedly from conventional emulsion chain polymers. This study examines how the change of polymerization mechanism affects polymer molecular weight, structure and composition. A 2,2′‐dimercaptodiethyl sulfide/diallyl phthalate emulsion is photopolymerized in a photochemical stirred‐tank reactor equipped with Light‐emitting diodes (LEDs) to yield a 30% solids content latex with a high weight‐average molecular weight (100 kDa) and a broad molecular weight distribution ( Đ = 8.5). Intramolecular cyclization occurs during polymerization by the addition of a thiyl radical to the unsaturated end group of the same molecule. Irreversible ring‐closure takes place to produce “dead” cyclic oligomers in the early stage of the reaction, whereas chain‐growth continues at high conversion. Consequently, the particles are composed of high molecular weight linear chains and a fraction of stable oligomer cycles, showing a broad and bimodal molecular weight distribution. The linear poly(thioether) chains include occasionally disulfide units due to thiyl radical recombination. The reversibility of disulfide bonds causes a decrease of molecular weight during storage. The addition of radical inhibitor to the latex stops fragmentation of SS bonds.