Uncontrolled side reactions during thioether and carbonate synthesis lead to low monomer purity and poor polymerization kinetics. These methods stabilize the chemical precursors to ensure consistent polymer backbone architecture.
Standard cyclic carbonate precursors lack the functional variety required for specialized polymerization pathways. Expanding the chemical space of reactive sulfur-containing monomers enables the synthesis of polymers with tailored refractive indices and degradability.